Huntington Willard

Huntington Willard's AcademicInfluence.com Rankings

Huntington Willard

Biology

#2880

World Rank

#4495

Historical Rank

Genetics

#246

World Rank

#295

Historical Rank

Molecular Biology

#349

World Rank

#356

Historical Rank

biology Degrees

Download Badge

Biology

Huntington Willard's Degrees

PhD Genetics University of Washington

Why Is Huntington Willard Influential?

(Suggest an Edit or Addition)

According to Wikipedia, Huntington Faxon Willard is an American geneticist. In 2014, he was named to head the Marine Biological Laboratory, and is a professor in human genetics at the University of Chicago. He stepped down from leading the lab in 2017 to return to research. Willard was elected to the National Academy of Medicine in 2016. Earlier, beginning in 2003 he was the Nanaline H. Duke Professor of Genome Sciences, the first director of the Institute for Genome Sciences and Policy, and Vice Chancellor for Genome Sciences at Duke University Medical Center in Durham, North Carolina.

(See a Problem?)

Huntington Willard's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

X-inactivation profile reveals extensive variability in X-linked gene expression in females (2005) (1828)
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome (1991) (1387)
The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus (1992) (1225)
The DNA sequence of the human X chromosome (2005) (1072)
Cloning of human androgen receptor complementary DNA and localization to the X chromosome. (1988) (975)
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules (1991) (804)
XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure (1996) (781)
Formation of de novo centromeres and construction of first-generation human artificial microchromosomes (1997) (636)
Report of the committee on the genetic constitution of the X chromosome. (1988) (570)
Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum. (1990) (551)
Hierarchical order in chromosome-specific human alpha satellite DNA (1987) (540)
Characterization of a murine gene expressed from the inactive X chromosome (1991) (525)
Genomic and personalized medicine: foundations and applications. (2009) (521)
Genomic and Genetic Definition of a Functional Human Centromere (2001) (475)
Uniparental disomy as a mechanism for human genetic disease. (1988) (466)
Clonal analysis using recombinant DNA probes from the X-chromosome. (1987) (457)
Homologous ribosomal protein genes on the human X and Y chromosomes: Escape from X inactivation and possible implications for turner syndrome (1990) (395)
Localization of the X inactivation centre on the human X chromosome in Xq13 (1991) (378)
Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism. (1989) (361)
A first-generation X-inactivation profile of the human X chromosome. (1999) (355)
Heritable Individual-Specific and Allele-Specific Chromatin Signatures in Humans (2010) (330)
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge (2014) (306)
Analysis of DNA Methylation in a Three-Generation Family Reveals Widespread Genetic Influence on Epigenetic Regulation (2011) (297)
X chromosome-inactivation patterns of 1,005 phenotypically unaffected females. (2006) (291)
The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1. (1993) (285)
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation (1997) (282)
The human X-inactivation centre is not required for maintenance of X-chromosome inactivation (1994) (281)
Centromeres of mammalian chromosomes. (1990) (256)
Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes. (1988) (256)
Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome (1986) (248)
Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome (1987) (241)
Isolation and characterization of a major tandem repeat family from the human X chromosome. (1983) (238)
PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs (1985) (233)
A Novel Chromatin Protein, Distantly Related to Histone H2a, Is Largely Excluded from the Inactive X Chromosome (2001) (233)
Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome. (2004) (230)
Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders. (2002) (221)
Gene encoding the beta subunit of S100 protein is on chromosome 21: implications for Down syndrome. (1988) (220)
Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability. (1989) (219)
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome. (1985) (219)
The UTX gene escapes X inactivation in mice and humans. (1998) (211)
A Heterochromatin Barrier Partitions the Fission Yeast Centromere into Discrete Chromatin Domains (2006) (209)
Development and application of a phylogenomic toolkit: resolving the evolutionary history of Madagascar's lemurs. (2008) (206)
Centromere reference models for human chromosomes X and Y satellite arrays (2013) (202)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms. (1989) (198)
Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders. (1985) (198)
Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes. (1987) (195)
Public knowledge of and attitudes toward genetics and genetic testing. (2013) (194)
X inactivation in females with X-linked disease. (1998) (192)
Expression of genes from the human active and inactive X chromosomes. (1997) (186)
Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant. (2001) (185)
Thompson & Thompson Genetics in Medicine (2007) (182)
Integration of human α-satellite DNA into simian chromosomes: Centromere protein binding and disruption of normal chromosome segregation (1992) (180)
Klinefelter syndrome: Expanding the phenotype and identifying new research directions (2003) (177)
Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome. (1985) (177)
Heritability of X chromosome--inactivation phenotype in a large family. (1996) (176)
Linear assembly of a human centromere on the Y chromosome (2018) (176)
Analysis of the centromeric regions of the human genome assembly. (2004) (173)
Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA. (1997) (166)
Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others. (1999) (157)
Five polymorphic microsatellite VNTRs on the human X chromosome. (1990) (157)
Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence. (1975) (153)
Effects of sequence variation on differential allelic transcription factor occupancy and gene expression (2012) (148)
Exome Sequencing–Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants (2018) (147)
Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study. (1991) (144)
An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells (2002) (143)
Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA. (1989) (142)
Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987). (1987) (138)
The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA. (1998) (131)
Chromosome-specific subsets of human alpha satellite DNA: Analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat (2005) (129)
Replication timing of DNA sequences associated with human centromeres and telomeres (1990) (128)
Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome. (2003) (126)
Mammalian chromosome structure. (1993) (125)
Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end. (1988) (125)
Evolution of alpha satellite. (1991) (125)
Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy. (1976) (123)
Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10. (1988) (122)
Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps. (1986) (120)
Report of the committee on human gene mapping by recombinant DNA techniques. (1987) (120)
Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes. (1984) (119)
Physical and genetic mapping of the human X chromosome centromere: repression of recombination. (1998) (118)
Thompson and Thompson Genetics in Medicine (2001) (118)
Cell cycle–dependent localization of macroH2A in chromatin of the inactive X chromosome (2002) (117)
Chromosome-specific organization of human alpha satellite DNA. (1985) (117)
Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene. (1997) (116)
Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease. (1986) (116)
The evolutionary dynamics of alpha-satellite. (2005) (114)
PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis. (1991) (112)
Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixation. (1986) (111)
Stable dicentric X chromosomes with two functional centromeres (1998) (111)
A national clinical decision support infrastructure to enable the widespread and consistent practice of genomic and personalized medicine (2009) (110)
Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status. (1992) (109)
Evolutionary conservation of possible functional domains of the human and murine XIST genes. (1993) (109)
Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant. (1978) (109)
A novel transmembrane transporter encoded by the XPCT gene in Xq13.2. (1994) (108)
The β-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus (1986) (103)
Alpha-satellite DNA and vector composition influence rates of human artificial chromosome formation. (2002) (102)
A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat loci. (1993) (102)
Evidence of Influence of Genomic DNA Sequence on Human X Chromosome Inactivation (2006) (98)
Genomic Characterization of Large Heterochromatic Gaps in the Human Genome Assembly (2014) (95)
Pulsed-field gel analysis of alpha-satellite DNA at the human X chromosome centromere: high-frequency polymorphisms and array size estimate. (1990) (95)
Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA. (1987) (94)
Genomic analysis of sequence variation in tandemly repeated DNA. Evidence for localized homogeneous sequence domains within arrays of alpha-satellite DNA. (1990) (92)
Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals. (1995) (90)
Genomic and personalized medicine (2009) (88)
Progressive proximal expansion of the primate X chromosome centromere. (2005) (88)
Sequences Associated with Centromere Competency in the Human Genome (2012) (87)
Centromeres: the missing link in the development of human artificial chromosomes. (1998) (86)
Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin (1993) (85)
Report of the committee on human gene mapping by recombinant DNA techniques. (1988) (84)
Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A. (1990) (84)
Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes. (1986) (83)
Beta satellite DNA: characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes. (1992) (83)
An assay for X inactivation based on differential methylation at the fragile X locus, FMR1. (1996) (81)
Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation. (1996) (81)
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations. (1994) (81)
Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation. (1998) (81)
Molecular Cloning of cDNA Encoding the Ca 2 + Release Channel ( Ryanodine Receptor ) of Rabbit Cardiac Muscle Sarcoplasmic Reticulum * (2001) (81)
Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation (1997) (80)
The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy. (1990) (78)
Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis). (1986) (78)
Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase. (1985) (78)
Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia. (1994) (76)
Report of the committee on the genetic constitution of the X chromosome (Part 1 of 7) (1991) (75)
Patterns of intra- and interarray sequence variation in alpha satellite from the human X chromosome: evidence for short-range homogenization of tandemly repeated DNA sequences. (1989) (75)
Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene. (1988) (74)
X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse. (1996) (74)
Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene. (1996) (74)
Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome (2001) (74)
Structure, sequence, expression, and chromosomal localization of the human V1a vasopressin receptor gene. (1996) (73)
Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16. (1989) (72)
Intracellular binding of radioactive hydroxocobalamin to cobalamin-dependent apoenzymes in rat liver. (1977) (72)
Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays. (1991) (71)
Isolation of human fibroblast catalase cDNA clones. Sequence of clones derived from spliced and unspliced mRNA. (1984) (69)
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. (1998) (68)
Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience. (2018) (68)
Genetic Control of X Chromosome Inactivation in Mice: Definition of the Xce Candidate Interval (2006) (68)
Structure of the rabbit phospholamban gene, cloning of the human cDNA, and assignment of the gene to human chromosome 6. (1991) (67)
Report of the Fourth International Workshop on human X chromosome mapping 1993 (1993) (66)
Genomic medicine: genetic variation and its impact on the future of health care (2005) (66)
Cobalamin coenzyme synthesis in normal and mutant human fibroblasts. Evidence for a processing enzyme activity deficient in cblC cells. (1979) (66)
Genetic linkage map of human chromosome 7 with 63 DNA markers. (1987) (65)
Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7. (1992) (65)
Deletions in Xq26.3–q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern (1997) (64)
Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome. (1991) (64)
An RNA Polymerase III-Dependent Heterochromatin Barrier at Fission Yeast Centromere 1 (2007) (64)
Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression. (1980) (64)
Purification and properties of methylmalonyl coenzyme A mutase from human liver. (1982) (64)
Study of V1-vascular Vasopressin Receptor Gene Microsatellite Polymorphisms in Human Essential Hypertension☆ (2000) (63)
Autosomal Dominant Mutations Affecting X Inactivation Choice in the Mouse (2002) (63)
Human T‐cell tumours containing chromosome 14 inversion or translocation with breakpoints proximal to immunoglobulin joining regions at 14q32. (1987) (63)
Artificial Chromosomes Coming to Life (2000) (62)
Assignment of human erythroid delta-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.21 by PCR analysis of somatic cell hybrids containing X; autosome translocations. (1992) (62)
X Chromosome Inactivation, XIST, and Pursuit of the X-Inactivation Center (1996) (62)
Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: A sensitive assay using cultured cells (1976) (61)
Inherited deficiencies of human methylmalonyl CaA mutase activity: reduced affinity of mutant apoenzyme for adenosylcobalamin. (1977) (58)
Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangement (1990) (58)
Artificial and engineered chromosomes: non-integrating vectors for gene therapy. (2005) (57)
Human Artificial Chromosomes with Alpha Satellite-Based De Novo Centromeres Show Increased Frequency of Nondisjunction and Anaphase Lag (2003) (57)
Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13. (1986) (57)
Genetic analysis of NF1: identification of close flanking markers on chromosome 17. (1987) (56)
Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect. (1989) (55)
Clinical outcomes of a genomic screening program for actionable genetic conditions (2020) (55)
Characterization of a chromosome-specific chimpanzee alpha satellite subset: evolutionary relationship to subsets on human chromosomes. (1996) (54)
Concerted evolution of primate alpha satellite DNA. Evidence for an ancestral sequence shared by gorilla and human X chromosome alpha satellite. (1990) (54)
The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene (1991) (54)
A primary genetic map of the pericentromeric region of the human X chromosome. (1988) (54)
Report of the fifth international workshop on human X chromosome mapping (1994) (53)
Rapid creation of BAC-based human artificial chromosome vectors by transposition with synthetic alpha-satellite arrays (2005) (53)
Chromosomal domains and escape from X inactivation: comparative X inactivation analysis in mouse and human (2000) (52)
X chromosome inactivation of the human TIMP gene. (1990) (52)
Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation. (1990) (51)
2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes. (1993) (51)
Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts. (1978) (49)
Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse. (1990) (49)
BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes (1976) (47)
Mammalian X-chromosome inactivation and the XIST gene. (1992) (46)
Mammalian X-chromosome inactivation and the XIST gene (1992) (45)
Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation. (1993) (45)
Genetic and physical mapping around the properdin P gene. (1991) (45)
Study of V(1)-vascular vasopressin receptor gene microsatellite polymorphisms in human essential hypertension. (2000) (44)
Personalized Health Planning (2003) (44)
Molecular cloning and chromosomal localization of DNA sequences associated with a human DNA repair gene (1985) (44)
Chromosomal location of human P-glycoprotein gene sequences. (1987) (44)
The DXS423E gene in Xp11.21 escapes X chromosome inactivation. (1995) (43)
Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST. (1993) (42)
Sequence organization and functional annotation of human centromeres. (2003) (42)
Barring gene expression after XIST: maintaining facultative heterochromatin on the inactive X. (2003) (42)
Chromosome-specific α-satellite DNA from the centromere of chimpanzee chromosome 4 (1997) (42)
Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM. (1992) (41)
Genome analysis and the human X chromosome. (1992) (40)
X inactivation of the FMR1 fragile X mental retardation gene. (1995) (40)
Engineered human dicentric chromosomes show centromere plasticity (2005) (40)
Breaking the silence in Rett syndrome (1999) (39)
Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation. (1999) (39)
Primate comparative genomics: lemur biology and evolution. (2007) (38)
Assignment of human gamma crystallin multigene family to chromosome 2 (1985) (38)
Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation. (1985) (38)
Efficient assembly of de novo human artificial chromosomes from large genomic loci (2005) (38)
Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant (2013) (38)
Concerted evolution of alpha satellite DNA: Evidence for species specificity and a general lack of sequence conservation among alphoid sequences of higher primates (1989) (37)
Organization and molecular cytogenetics of a satellite DNA family fromHoplias malabaricus (Pisces, Erythrinidae) (1993) (36)
Allele-specific distribution of RNA polymerase II on female X chromosomes. (2011) (36)
Organization, polymorphism, and molecular cytogenetics of chromosome-specific alpha-satellite DNA from the centromere of chromosome 2. (1992) (36)
Essentials Of Genomic And Personalized Medicine (2010) (36)
Genetic and parent-of-origin influences on X chromosome choice in Xce heterozygous mice (2005) (36)
Interhomologue sequence variation of alpha satellite DNA from human chromosome 17: Evidence for concerted evolution along haplotypic lineages (1995) (35)
Organization and evolution of alpha satellite DNA from human chromosome 11 (2004) (34)
An 18-locus linkage map of the pericentromeric region of the human X chromosome: genetic framework for mapping X-linked disorders. (1991) (34)
Assembly and characterization of heterochromatin and euchromatin on human artificial chromosomes (2004) (34)
Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7. (1989) (33)
Chromosomal localization of the human homeo box-containing genes, EN1 and EN2. (1989) (33)
Remodelling chromatin with RNA (1997) (32)
Direct regional assignment of the gene for vitamin D binding protein (Gc-globulin) to human chromosome 4q11-q13 and identification of an associated DNA polymorphism (1986) (32)
Isolation and characterization of cloned human DNA fragments carrying reiterated sequences common to both autosomes and the X chromosome. (1981) (31)
A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes. (1995) (31)
Considerations for the Impact of Personal Genome Information: A Study of Genomic Profiling among Genetics and Genomics Professionals (2010) (31)
Chromosome-wide, allele-specific analysis of the histone code on the human X chromosome. (2006) (31)
Tissue-specific heterogeneity in DNA replication patterns of human X chromosomes (1977) (31)
A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status. (1996) (31)
Expression-based assay of an X-linked gene to examine effects of the X-controlling element (Xce) locus (2000) (30)
Genomic and epigenomic approaches to the study of X chromosome inactivation. (2006) (30)
X chromosome inactivation and X-linked mental retardation. (1996) (30)
Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: implications for linkage in neurofibromatosis. (1987) (28)
Human artificial chromosomes: potential applications and clinical considerations. (2006) (28)
Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19 (2004) (28)
Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girl (1990) (28)
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization (1990) (28)
Centromeres of human chromosomes (1996) (27)
Report of the committee on the genetic constitution of the X chromosome (Part 1 of 3) (1990) (27)
Refined localization of human connexin32 gene locus, GJB1, to Xq13.1. (1992) (26)
Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin. (1992) (26)
Nonrandom X Chromosome Inactivation Is Influenced by Multiple Regions on the Murine X Chromosome (2012) (26)
Molecular cytogenetics of alpha satellite DNA from chromosome 12: fluorescence in situ hybridization and description of DNA and array length polymorphisms. (1991) (25)
Molecular analysis of gene deletion in aniridia-Wilms tumor association (1985) (25)
The genomics of long tandem arrays of satellite DNA in the human genome. (1989) (25)
Genome biology: Tales of the Y chromosome (2003) (25)
Defining the spectrum of genome policy (2006) (25)
PCR amplification of tandemly repeated DNA: analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA. (1992) (25)
Human genomics: In search of normality (2006) (25)
An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse. (2003) (24)
Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization. (1993) (24)
Genetics of Common Disorders with Complex Inheritance (2007) (24)
Impact of Delivery Models on Understanding Genomic Risk for Type 2 Diabetes (2014) (24)
The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints. (1989) (24)
Human centromere structure: organization and potential role of alpha satellite DNA. (1989) (24)
Molecular and Genetic Studies of Human X Chromosome Inactivation (1993) (23)
Abstracts of workshop presentations (Part 13 of 13) (1985) (23)
Linkage of cystic fibrosis to the pro alpha 2(I) collagen gene, COL1A2, on chromosome 7. (1986) (23)
The common acute lymphoblastic leukemia antigen (neutral endopeptidase-3.4.24.11) gene is located on human chromosome 3. (1989) (23)
Chromosome engineering: generation of mono- and dicentric isochromosomes in a somatic cell hybrid system (1999) (23)
Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies. (1993) (22)
Chromosome-specific alpha-satellite DNA from the centromere of chimpanzee chromosome 4. (1997) (22)
Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts. (1980) (22)
A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes. (1991) (22)
Composition and organization of active centromere sequences in complex genomes (2012) (22)
The Impact of Local Genome Sequence on Defining Heterochromatin Domains (2009) (21)
Seventh International Workshop on the Fragile X and X-linked Mental Retardation. (1996) (21)
Report of the committee on the genetic constitution of the X chromosome. (1988) (21)
Abstracts of workshop presentations (Part 2 of 16) (1987) (20)
Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm. (1991) (20)
Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosome. (1987) (20)
Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques. (1985) (20)
Interferon-regulated human 2–5A synthetase gene maps to chromosome 12 (1986) (19)
Abstracts of workshop presentations (Part 6 of 16) (1987) (19)
The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysis (1990) (19)
Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993. (1993) (19)
Principles of Clinical Cytogenetics (2007) (19)
Organization and Molecular Evolution of CENP-A–Associated Satellite DNA Families in a Basal Primate Genome (2011) (18)
Localization of histidase to human chromosome region 12q22----q24.1 and mouse chromosome region 10C2----D1. (1991) (18)
Orangutan α-satellite monomers are closely related to the human consensus sequence (1998) (18)
Clinical objectives in medical genetics for undergraduate medical students (1998) (18)
Mapping of the cystic fibrosis locus on chromosome 7. (1986) (17)
Centromeres--primary constrictions are primarily complicated. (1992) (17)
Counting on Xist (1998) (17)
Uncoupling of Genomic and Epigenetic Signals in the Maintenance and Inheritance of Heterochromatin Domains in Fission Yeast (2012) (17)
Chromosome manipulation: a systematic approach toward understanding human chromosome structure and function. (1996) (17)
Organization and evolution of an alpha satellite DNA subset shared by human chromosomes 13 and 21 (1993) (17)
Genetic analysis of eight loci tightly linked to neurofibromatosis 1. (1989) (17)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 782–806 (1989) (16)
Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus. (2011) (16)
Human X chromosomes: Synchrony of DNA replication in diploid and triploid fibroblasts with multiple active or inactive X chromosomes (1980) (16)
Interactions of methylmalonyl CoA mutase from normal human fibroblasts with adenosylcobalamin and methylmalonyl CoA: evidence for non-equivalent active sites. (1980) (16)
Genetic linkage analysis of the pericentromeric region of the human x chromosome using polymorphic alpha satellite dna (1987) (16)
Gene for lipoamide dehydrogenase maps to human chromosome 7 (1988) (16)
Gene on short arm of human X chromosome complements murine tsA1S9 DNA synthesis mutation (1989) (16)
Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation. (1994) (15)
Letting the genome out of the bottle. (2008) (15)
Neocentromeres and human artificial chromosomes: An unnatural act (2001) (15)
Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patients with androgen insensitivity and mental retardation. (2000) (15)
Regional localization of the TIMP gene on the human X chromosome (1989) (15)
Clinical Cytogenetics: Disorders of the Autosomes and the Sex Chromosomes (2007) (15)
Organization, Variation and Expression of the Human Genome (2010) (15)
Human artificial chromosomes coming into focus (1998) (15)
Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques. (1984) (15)
Orangutan alpha-satellite monomers are closely related to the human consensus sequence. (1998) (15)
A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma. (1992) (14)
Report of the committee on the genetic constitution of the X chromosome. (1990) (14)
Chromosome specificity of satellite DNAs: short- and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3 (1989) (14)
Rapid creation of BAC-based human artifical chromosome vectors by transposition with synthetic alpha-satellite arrays (2005) (14)
Patterns of Single-Gene Inheritance (2007) (14)
CHAPTER 1 – Organization, Variation and Expression of the Human Genome as a Foundation of Genomic and Personalized Medicine (2009) (13)
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers. (1990) (13)
Organization and genomic distribution of “82H” alpha satellite DNA (2004) (13)
Abstracts of workshop presentations (Part 1 of 13) (1985) (13)
The evolutionary dynamics of (cid:1) -satellite (2005) (13)
A centromere-based linkage group on the long arm of human chromosome 17. (1988) (11)
Personalized Genetic Medicine (2007) (11)
Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11 (1987) (11)
Inborn errors of cobalamin metabolism: Effect of cobalamin supplementation in culture on methylmalonyl CoA mutase activity in normal and mutant human fibroblasts (1979) (10)
Pulsed-field map of Xq13 in the region of the human X inactivation center. (1993) (10)
Evidence for sequence biases associated with patterns of histone methylation (2012) (10)
The Foundations of Genomic and Personalized Medicine (2010) (10)
Pulsed-field and two-dimensional gel electrophoresis of long arrays of tandemly repeated DNA : analysis of human centromeric alpha satellite. (1992) (10)
Abstracts of workshop presentations (Part 9 of 13) (1985) (10)
RFLP detected by an X-linked cDNA encoding erythroid-potentiating activity/tissue inhibitor of metalloproteinase (EPA/TIMP). (1986) (10)
The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation. (1995) (10)
Abstracts of workshop presentations (Part 12 of 16) (1987) (10)
Abstracts of meeting presentations (Part 11 of 11) (1984) (10)
Localization of the insulin receptor-related receptor gene to human chromosome 1. (1990) (9)
Linear Assembly of a Human Y Centromere using Nanopore Long Reads (2017) (9)
Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction (1989) (9)
SETting the stage. Eed-Enx1 leaves an epigenetic signature on the inactive X chromosome. (2003) (9)
Regular ArticleThe CEPH Consortium Linkage Map of Human Chromosome 11 (1995) (9)
Report of the committee on the genetic constitution of the X chromosome (Part 7 of 7) (1991) (9)
MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA clone. (1987) (9)
Further linkage studies between retinoschisis and cloned dna sequences from the distal xp (1985) (9)
Abstracts of workshop presentations (Part 12 of 13) (1985) (9)
Protein kinase C: a new linkage marker for growth hormone and for COL1A1. (1989) (8)
Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994. (1994) (8)
Abstracts of workshop presentations (Part 15 of 16) (1987) (8)
Principles of Molecular Disease: Lessons from the Hemoglobinopathies (2007) (8)
Abstracts of workshop presentations (Part 10 of 16) (1987) (7)
A genomic search for linkage of neurofibromatosis to RFLPs. (1987) (7)
Abstracts of workshop presentations pp. 1040-1056 (1989) (6)
The Treatment of Genetic Disease (2007) (6)
An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22 [HGM8 provisional no. DXS72]. (1985) (6)
Molecular organization of repeated dna sequences on the human y chromosome (1985) (6)
Abstracts of meeting presentations (Part 2 of 11) (1982) (6)
The Molecular, Biochemical, and Cellular Basis of Genetic Disease (2007) (6)
PstI RFLP in the human hexosaminidase (HEXB) gene on chromosome 5. (1987) (5)
Isolation, characterization and chromosomal localization of cDNA clones for the E1β subunit of the pyruvate dehydrogenase complex (1990) (5)
Abstracts of meeting presentations (Part 8 of 11) (1984) (5)
Abstracts of workshop presentations pp. 948-967 (1989) (5)
Abstracts of meeting presentations (Part 10 of 11) (1984) (5)
Abstracts of workshop presentations pp. 1023-1039 (1989) (5)
Genetic Variation in Individuals and Populations: Mutation and Polymorphism (2007) (5)
MspI RFLP detected with chromosome-walk clone pXUT23-SE3.2L from DXS16 in Xp22.1-22.3. (1987) (5)
Calendar of Events: 1991 — 1992 (1991) (4)
Genome maps III. 1992. Wall Chart. (1992) (4)
Two Ca2+ ATPase genes+ (1986) (4)
ORNITHINE AMINOTRANSFERASE (OAT): EVIDENCE FOR A DISPERSED GENE FAMILY WITH MEMBER(S) LOCALIZED TO Xp11.1 – Xp21.1 (1987) (4)
Abstracts of workshop presentations (Part 7 of 16) (1987) (4)
Pericentromeric structure of human X “isochromosomes”: evidence for molecular heterogeneity (1990) (4)
A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids (2004) (4)
Report of the committee on the genetic constitution of the X chromosome (Part 6 of 7) (1991) (4)
Abstracts of workshop presentations (Part 3 of 16) (1987) (4)
Abstracts of workshop presentations (Part 1 of 16) (1987) (4)
Abstracts of workshop presentations pp. 1057-1074 (1989) (4)
Report of the committee on the genetic constitution of the X chromosome (Part 3 of 3) (1989) (4)
Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1' (1989) (4)
Molecular Heterogeneity in O-Variant GM2 Gangliosidosis (1986) (3)
Abstracts of workshop presentations (Part 4 of 16) (1987) (3)
The Human Genome and the Chromosomal Basis of Heredity (2007) (3)
Evidence for a chromosomal breakage hotspot in a 3 Mb region of Xp11.21 (1994) (3)
Abstracts of workshop presentations (Part 11 of 13) (1985) (3)
The Human Genome: Gene Structure and Function (2007) (3)
Gene order on the short arm of human chromosome 11: regional assignment of the LDH A gene distal to catalase in two translocations (2004) (3)
Clinical validation of genomic functional screen data: Analysis of observed BRCA1 variants in an unselected population cohort (2022) (3)
Abstracts of workshop presentations (Part 8 of 16) (1987) (3)
Abstracts of workshop presentations pp. 1075-1091 (1989) (3)
Competencies: a cure for pre-med curriculum. (2011) (2)
A Rsal RFLP at the DXS467 locus. (1990) (2)
Abstracts of workshop presentations (Part 4 of 13) (1985) (2)
A BstE II RFLP at the DXS153 locus. (1990) (2)
Abstracts of workshop presentations (Part 5 of 16) (1987) (2)
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge (2014) (2)
Cancer Genetics and Genomics (2007) (2)
Alpha and beta satellite sequences on chromosome 21: the possible role of centromere and chromosome structure in nondisjunction. (1990) (2)
Evolution and function of alpha satellite DNA (2001) (2)
Fast-twitch and slow-twitch/cardiac Ca2+ ATPase genes map to human chromosomes 16 and 12 (1988) (2)
The needle found!!! Trinucleotide repeat expansion in the Huntington's disease gene. (1993) (2)
Abstracts of workshop presentations pp. 1106-1116 (1989) (2)
Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome (1988) (2)
Clinical Case Studies Illustrating Genetic Principles (2007) (2)
2001 ASHG Presidential Address. On black boxes and storytellers: lessons learned in human genetics. (2002) (2)
Isolation, characterization and chromosomal localization of cDNA clones for the E1 beta subunit of the pyruvate dehydrogenase complex. (1990) (2)
Genetic Counseling and Risk Assessment (2007) (2)
Abstracts of workshop presentations (Part 14 of 16) (1987) (2)
Abstracts of workshop presentations (Part 11 of 16) (1987) (2)
Abstracts of meeting presentations (Part 6 of 11) (1984) (1)
On Black Boxes and Storytellers: Lessons Learned in Human Genetics * * Previously presented at the a (2002) (1)
2009 William Allan Award Address: Life in The Sandbox: Unfinished Business (2010) (1)
Alexander F. Zakharov (1986) (1)
Composition and organization of active centromere sequences in complex genomes (2012) (1)
Abstracts of workshop presentations (Part 5 of 13) (1985) (1)
Abstracts of workshop presentations (Part 16 of 16) (1987) (1)
Cloning of the X-linked glycerol kinase gene. (1993) (1)
Mammalian genetics Editorial overview: a sampler of current opinion (1993) (1)
In memory of Samuel A. Latt, M.D., Ph.D. (1989) (1)
The Science of Genetics: An Introduction to Heredity. Third Edition (1978) (1)
Ethical Issues in Medical Genetics (2007) (1)
Methods for “ The effects of genome sequence on differential allelic transcription factor occupancy and gene expression ” (2012) (1)
Abstracts of workshop presentations (Part 7 of 13) (1985) (1)
An X-linked DraI RFLP recognized by cpX23 [DXS132]. (1989) (1)
Abstracts of workshop presentations (Part 9 of 16) (1987) (1)
GENETIC AND PHYSICAL MAPPING AROUND THE RETINITIS-PIGMENTOSA (RP2) LOCUS IN XP11.23 (1991) (1)
Evidence for sequence biases associated with patterns of histone methylation (2012) (1)
Onrginal articles X inactivation of the FMR 1 fragile X mental retardation gene (1)
Abstracts of workshop presentations (Part 6 of 13) (1985) (1)
Abstracts of workshop presentations (Part 2 of 13) (1985) (1)
Abstracts of meeting presentations (Part 9 of 11) (1984) (1)
Contents Vol. 55, 1990 (1990) (1)
Developmental Genetics and Birth Defects (2007) (1)
Human X Chromosome (2000) (0)
Abstracts of workshop presentations pp. 1006-1022 (1989) (0)
Human Gene Mapping and Disease Gene Identification (2007) (0)
Genetics of disease. (1995) (0)
Subject Index Vol. 64, 1993 (1993) (0)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 758–781 (1989) (0)
Cloning of the breakpoint in the 10 14 translocation of t cell neoplasia and identification of a chromosome 10 specific sequence (1989) (0)
Report of the committee on the genetic constitution of the X chromosome (Part 2 of 3) (1989) (0)
Abstracts of meeting presentations (Part 7 of 11) (1984) (0)
Letter to the Editor -1 Immunophenotyping and Molecular Cytogenetics (1992) (0)
Genetic Complementation amongInherited Deficiencies of Methylmalonyl-CoA MutaseActivity: Evidence foraNewClass ofHumanCobalamin Mutant (1978) (0)
Thompson And Thompso genetics in medicine (2013) (0)
Clinical outcomes of a genomic screening program for actionable genetic conditions (2020) (0)
Commentary Chromosome manipulation: A systematic approach toward understanding human chromosome structure and function (2005) (0)
Subject Index Vol. 56, 1991 (1991) (0)
Abstract of papers presented at the Third International Symposium on Myelodysplastic SyndromesAbsence of the X1st gene from the late replicating isodicentric X chromosome in myelodysplasia (1994) (0)
Contents, Vol. 46, 1987/ Title Page / Table of Contents (1987) (0)
Comprar The Book of Genes & Genomes | Haga, Susanne | 9780387709154 | Springer (2008) (0)
Signatures in Humans Heritable Individual-Specific and Allele-Specific Chromatin (2011) (0)
Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant (2013) (0)
The Histochemical Society Annual Meeting (1996) (0)
The genome for the masses (2005) (0)
Mapping of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse (1994) (0)
The inv(16) in acute nonlymphocytic leukemia: a turnabout for myosin heavy chain. (1993) (0)
Eleventh International Chromosome Conference (2004) (0)
A letter response to Chaufan's "how much can a large population study on genes, environments, their interactions and common diseases contribute to the health of the American people?" (65:8, 2007, 1730-1741). (2008) (0)
Two PstI RFLPs in the PCCB gene on the long arm of chromosome 3. (1988) (0)
Subject index Vol. 40, 1985 (1985) (0)
Introductory Speech for David Page (2004) (0)
2015 ASHG Awards and Addresses. (2016) (0)
Nucleic Acids Research Nudeotide sequence heterogeneity of alpha satellite repetitive DNA : a survey of alphold sequences from different human chromosomes (2005) (0)
Report of the committee on the genetic constitution of the X chromosome (Part 4 of 7) (1991) (0)
Replication Timing ofDNA Sequences Associated withHuman Centromeres andTelomeres (1990) (0)
The Human Genome (2013) (0)
Abstracts of workshop presentations (Part 8 of 13) (1985) (0)
You say tomato and I say tomahto: human genetics and gene therapy. (2001) (0)
Molecular Cloning and Chromosomal Localization of DNA Sequences Associated with a Human DNA (2003) (0)
Complete sequence representation across human X and Y centromeric regions (2013) (0)
GENETIC AND PHYSICAL MAPPING AROUND THE RP2-LOCUS IN XP11.23 (1991) (0)
Abstracts of meeting presentations (Part 4 of 11) (1979) (0)
Abstract (2001) (0)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 732–757 (1989) (0)
Abstracts of workshop presentations (Part 13 of 16) (1987) (0)
Listing of forthcoming and published papers available on line (1989) (0)
SHORT COMMUNICATION Refined Localization of Human Connexin32 Gene Locus, GJBI, to Xql3.1 (1992) (0)
Thampson & Thampson Genetics in Medicine (2012) (0)
Honest Jim talks manners (2007) (0)
Welcome to the Genome: A User's Guide to the Genetic Past, Present and Future By Rob DeSalle and Michael Yudell (2005) (0)
Subject Index Vol. 41, 1986 (2004) (0)
Chromosome synthetique de mammifere et procedes de construction de celui-ci (1996) (0)
The Human Genome: Foundation for Genomic and Precision Medicine (2017) (0)
Index by Keyword (1989) (0)
Report of the committee on the genetic constitution of the X chromosome (Part 3 of 7) (1991) (0)
Tools of Human Molecular Genetics (2007) (0)
Title Page / Table of Contents / Abstracts (1991) (0)
Abstracts of meeting presentations (Part 1 of 11) (1982) (0)
samuel pruzansky memorial lecture (1999) (0)
Report of the committee on the genetic constitution of the X chromosome (Part 2 of 7) (1991) (0)
Genome discoveries and clinical applications (2009) (0)
Contents, Vol. 56, 1991 (2004) (0)
Guidelines for interpreting abbreviations and specialized phrases in committee text and tables (1989) (0)
Principles, methodology and translational approaches (2009) (0)
An X-linked homologue of the autosomal inprinted gene ZNF127 escapes X inactivation (1994) (0)
Subject index Vol. 46, 1987 (1987) (0)
A note on the use of HGML LIT literature file numbers (1989) (0)
Contents, Vol. 37, 1984 (1984) (0)
The human genome as a foundation for genomic and precision health (2019) (0)
90 Detection of chromosomal aberrations in interphase nuclei from human primary breast tumors using in situ hybridization with chromosome-specific repetitive DNA-probes (1989) (0)
Uniparental Disomyas a Mechanism forHuman Genetic Disease (1988) (0)
Genetics and Genomics in Medicine. By Tom Strachan, Judith Goodship, and Patrick Chinnery. New York: Garland Science (Taylor & Francis Group). $125.00 (paper). xvii + 526 p.; ill.; index. ISBN: 978-0-8153-4480-3. 2015. (2016) (0)
Report of the committee on the genetic constitution of the X chromosome (Part 5 of 7) (1991) (0)
Index by Abstract Number (1989) (0)
Abstracts of workshop presentations (Part 10 of 13) (1985) (0)
The Histochemical Society Annual Meeting (1997) (0)

This paper list is powered by the following services:

Other Resources About Huntington Willard

en.wikipedia.org

What Schools Are Affiliated With Huntington Willard?

Huntington Willard is affiliated with the following schools:

Huntington Willard's Academic­Influence.com Rankings

Huntington Willard's Degrees

Why Is Huntington Willard Influential?

Huntington Willard's Published Works

Published Works

Other Resources About Huntington Willard

What Schools Are Affiliated With Huntington Willard?

Huntington Willard's AcademicInfluence.com Rankings