Norman Arnheim | Academic Influence

Norman Arnheim's AcademicInfluence.com Rankings

Norman Arnheim

Biology

#1264

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#2145

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Molecular Biology

#168

World Rank

#172

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Cell Biology

#282

World Rank

#290

Historical Rank

Genetics

#475

World Rank

#546

Historical Rank

biology Degrees

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Biology

Norman Arnheim's Degrees

PhD Biology University of California, Berkeley
Masters Biology University of California, Berkeley
Bachelors Biology University of California, Berkeley

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Why Is Norman Arnheim Influential?

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According to Wikipedia, Norman Arnheim is an American biologist specializing in aging and development biology, biochemistry, and molecular biology. He is currently a Distinguished Professor and the Ester Dornsife Chair at the University of Southern California, and an Elected Fellow of the American Association for the Advancement of Science.

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Norman Arnheim'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

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. (1985) (8169)
Most human carcinomas of the exocrine pancreas contain mutant c-K-ras genes (1988) (2173)
Enzymatic amplification of ?-globin genomic sequences and restriction site analysis for diagnosis of (1985) (1168)
Whole genome amplification from a single cell: implications for genetic analysis. (1992) (946)
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over (1996) (821)
Detection of a specific mitochondrial DNA deletion in tissues of older humans. (1990) (760)
Detection of human papilloma virus in paraffin-embedded tissue using the polymerase chain reaction (1988) (721)
Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. (2004) (713)
Amplification and analysis of DNA sequences in single human sperm and diploid cells (1988) (669)
A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues. (1992) (630)
A simple method for site-directed mutagenesis using the polymerase chain reaction. (1989) (573)
Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis (1995) (557)
Hydroxylated quantum dots as luminescent probes for in situ hybridization. (2001) (554)
Polyglutamine-Expanded Human Huntingtin Transgenes Induce Degeneration of Drosophila Photoreceptor Neurons (1998) (528)
Molecular evidence for genetic exchanges among ribosomal genes on nonhomologous chromosomes in man and apes. (1980) (430)
Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain (1992) (402)
Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DMA mismatch repair (1998) (376)
Length mutations in human mitochondrial DNA: direct sequencing of enzymatically amplified DNA. (1987) (362)
Extension of base mispairs by Taq DNA polymerase: implications for single nucleotide discrimination in PCR. (1992) (356)
Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm. (2006) (306)
Taq DNA polymerase slippage mutation rates measured by PCR and quasi-likelihood analysis: (CA/GT)n and (A/T)n microsatellites. (2003) (300)
Detection of cytomegalovirus DNA in peripheral blood of patients infected with human immunodeficiency virus. (1988) (289)
A multiple-tubes approach for accurate genotyping of very small DNA samples by using PCR: statistical considerations. (1992) (233)
Polymerase chain reaction strategy. (1992) (228)
Deleterious mitochondrial DNA mutations accumulate in aging human tissues. (1992) (213)
Analysis of DNA sequences in forty-year-old paraffin-embedded thin-tissue sections: a bridge between molecular biology and classical histology. (1988) (207)
Triplet repeats form secondary structures that escape DNA repair in yeast. (1999) (207)
Detection of Human Papillomavirus in Formalin‐Fixed, Invasive Squamous Carcinomas Using the Polymerase Chain Reaction (1989) (203)
Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. 1985. (1992) (197)
Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers. (1989) (195)
5′ Flanking region of immunoglobulin heavy chain constant region genes displays length heterogeneity in germlines of inbred mouse strains (1980) (188)
Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain. (2007) (182)
Use of pooled DNA samples to detect linkage disequilibrium of polymorphic restriction fragments and human disease: studies of the HLA class II loci. (1985) (161)
Different mutator phenotypes in Mlh1- versus Pms2-deficient mice. (1999) (145)
Differential Contributions of Mammalian Rad54 Paralogs to Recombination, DNA Damage Repair, and Meiosis (2006) (142)
The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect (2002) (142)
Detection of c-K-ras mutations in fine needle aspirates from human pancreatic adenocarcinomas. (1990) (141)
New HLA–DPB1 alleles generated by interallelic gene conversion detected by analysis of sperm (1995) (139)
The evolutionarily conserved repetitive sequence d(TG.AC)n promotes reciprocal exchange and generates unusual recombinant tetrads during yeast meiosis. (1986) (138)
Transient reversion of ras oncogene-induced cell transformation by antibodies specific for amino acid 12 of ras protein (1985) (136)
Nup50, a Nucleoplasmically Oriented Nucleoporin with a Role in Nuclear Protein Export (2000) (135)
Direct electrophoretic detection of the allelic state of single DNA molecules in human sperm by using the polymerase chain reaction. (1990) (131)
Understanding what determines the frequency and pattern of human germline mutations (2009) (124)
Characterization of mouse ribosomal gene fragments purified by molecular cloning. (1979) (121)
Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping. (2000) (119)
Heterogeneity of the ribosomal genes in mice and men (1977) (116)
Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene (1994) (112)
Huntington disease expansion mutations in humans can occur before meiosis is completed (2003) (111)
Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism. (1999) (108)
Gene Targeting in Rat Embryo Fibroblasts Promoted by the Polyomavirus Large T Antigen Associated With Neurological Diseases (1996) (103)
Rapid prenatal diagnosis of sickle cell anemia by a new method of DNA analysis. (1987) (101)
Hot and cold spots of recombination in the human genome: the reason we should find them and how this can be achieved. (2003) (101)
Contributions by MutL homologues Mlh3 and Pms2 to DNA mismatch repair and tumor suppression in the mouse. (2005) (101)
Bacteriophage T7 lysozyme is an N-acetylmuramyl-L-alanine amidase. (1973) (100)
Mammalian meiotic recombination hot spots. (2007) (96)
Detection of human papillomavirus in normal and dysplastic tissue by the polymerase chain reaction. (1988) (91)
Human nucleolus organizers on nonhomologous chromosomes can share the same ribosomal gene variants. (1981) (90)
Species-specific rDNA transcription is due to promoter-specific binding factors (1984) (90)
Application of PCR: Organismal and Population BiologyPolymerase chain reaction can produce large quantities of specific DNA from small, degraded, and impure samples (1990) (85)
High resolution localization of recombination hot spots using sperm typing (1994) (84)
The genetic behaviour of a cloned mouse ribosomal DNA segment mimics mouse ribosomal gene evolution. (1979) (84)
Quantitative Immunological Comparison of Bird Lysozymes (1967) (81)
Using PCR in preimplantation genetic disease diagnosis. (1991) (79)
High-Resolution Recombination Patterns in a Region of Human Chromosome 21 Measured by Sperm Typing (2006) (77)
Widespread distribution of lysozyme g in egg white of birds. (1974) (77)
Amino acid sequence studies on bobwhite quail egg white lysozyme. (1972) (77)
Distribution of ribosomal gene length variants among mouse chromosomes. (1982) (76)
A germ-line-selective advantage rather than an increased mutation rate can explain some unexpectedly common human disease mutations (2008) (73)
Immunological prediction of sequence differences among proteins. Chemical comparison of chicken, quail, and phesant lysozymes. (1969) (73)
Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm (2006) (73)
Stability of intrastrand hairpin structures formed by the CAG/CTG class of DNA triplet repeats associated with neurological diseases. (1996) (73)
Close linkage between bovine prolactin and BoLA-DRB3 genes: genetic mapping in cattle by single sperm typing. (1992) (72)
DNase I-hypersensitive sites and transcription factor-binding motifs within the mouse E beta meiotic recombination hot spot (1991) (72)
Genetic analysis using the polymerase chain reaction. (1992) (72)
The Molecular Anatomy of Spontaneous Germline Mutations in Human Testes (2007) (67)
Individual variation in recombination among human males. (1996) (66)
Analysis of DNA sequence variation in single cells (1991) (65)
CAG repeat length variation in sperm from a patient with Kennedy's disease. (1995) (62)
Identification of the in vivo and in vitro origin of transcription in human rDNA (1982) (60)
Base mispair extension kinetics. Binding of avian myeloblastosis reverse transcriptase to matched and mismatched base pair termini. (1992) (60)
Linkage disequilibrium in human ribosomal genes: implications for multigene family evolution. (1988) (59)
The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing. (1997) (57)
Human immunodeficiency viral DNA is readily found in lymph node biopsies from seropositive individuals. Analysis of fixed tissue using the polymerase chain reaction. (1989) (57)
Positive Selection for New Disease Mutations in the Human Germline: Evidence from the Heritable Cancer Syndrome Multiple Endocrine Neoplasia Type 2B (2012) (57)
Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis? (1994) (56)
The Ups and Downs of Mutation Frequencies during Aging Can Account for the Apert Syndrome Paternal Age Effect (2009) (55)
Antibodies specific for amino acid 12 of the ras oncogene product inhibit GTP binding. (1985) (53)
The polymerase chain reaction. (1990) (53)
Mouse rDNA nontranscribed spacer sequences are found flanking immunoglobulin CH genes and elsewhere throughout the genome (1980) (53)
A member of a new repeated sequence family which is conserved throughout eucaryotic evolution is found between the human delta and beta globin genes. (1981) (51)
New evidence for positive selection helps explain the paternal age effect observed in achondroplasia (2013) (51)
PCR analysis of DNA sequences in single cells: single sperm gene mapping and genetic disease diagnosis. (1990) (50)
Nucleotide sequence of the genetically labile repeated elements 5' to the origin of mouse rRNA transcription (1983) (50)
A Novel Method for the Detection of Polymorphic Restriction Sites by Cleavage of Oligonucleotide Probes: Application to Sickle-Cell Anemia (1985) (49)
Polymorphisms in the human DNA repair gene XPF. (1999) (47)
Incomplete dosage compensation in an evolving Drosophila sex chromosome. (1978) (47)
Fine-structure genetic mapping of human chromosomes using the polymerase chain reaction on single sperm: experimental design considerations. (1989) (46)
Age-dependent germline mosaicism of the most common noonan syndrome mutation shows the signature of germline selection. (2013) (46)
cDNA cloning and characterization of Npap60: a novel rat nuclear pore-associated protein with an unusual subcellular localization during male germ cell differentiation. (1997) (45)
Chemical studies on the enzymatic specificity of goose egg white lysozyme. (1973) (43)
DNA mismatch repair in mammals: role in disease and meiosis. (1997) (43)
The mutation rate of the human mtDNA deletion mtDNA4977. (1996) (43)
Structure and organization of the highly repeated and interspersed 1.3 kb EcoRI-Bg1II sequence family in mice. (1980) (42)
Immunochemical resemblance between human leukemia and hen egg-ehite lysozyme and their reduced carboxymethyl derivatives. (1971) (41)
Multiple genes for lysozyme in birds. (1970) (40)
Detection of activated Mr 21,000 protein, the product of ras oncogenes, using antibodies with specificity for amino acid 12. (1986) (40)
Ordering three DNA polymorphisms on human chromosome 3 by sperm typing. (1991) (39)
Genetic Instability Induced by Overexpression of DNA Ligase I in Budding Yeast (2005) (39)
Length heterogeneity in a region of the human ribosomal gene spacer is not accompanied by extensive population polymorphism. (1978) (39)
Analysis of meiotic segregation, using single-sperm typing: meiotic drive at the myotonic dystrophy locus. (1996) (39)
Unequal exchange at the Charcot-Marie-Tooth disease type 1A recombination hot-spot is not elevated above the genome average rate. (2000) (38)
A new source of polymorphic DNA markers for sperm typing: analysis of microsatellite repeats in single cells. (1992) (38)
Multiple genes for lysozyme in birds. Studies on black swan egg white lysozymes. (1973) (38)
A novel repeat structure at the myotonic dystrophy locus in a 37 repeat allele with unexpectedly high stability. (1995) (38)
Isozymes of lysozyme in leukocytes and egg white: evidence for the species-specific control of egg-white lysozyme synthesis. (1974) (36)
Candidate DNA replication initiation regions at human trinucleotide repeat disease loci. (2003) (36)
Non-Darwinian Evolution: Consequences for Neutral Allelic Variation (1969) (36)
Detection and quantification of mitochondrial DNA deletions. (1996) (33)
Recombination hot spot in the human beta-globin gene cluster: meiotic recombination of human DNA fragments in Saccharomyces cerevisiae (1985) (33)
Multipoint mapping calculations for sperm-typing data. (1994) (31)
Germline Stem Cell Competition, Mutation Hot Spots, Genetic Disorders, and Older Fathers. (2016) (31)
Whole genome amplification of single cells: mathematical analysis of PEP and tagged PCR. (1995) (30)
Preimplantation diagnosis of genetic and chromosomal disorders (1994) (30)
Using the polymerase chain reaction to estimate mutation frequencies and rates in human cells. (1992) (29)
Mouse Strains with an Active H2-Ea Meiotic Recombination Hot Spot Exhibit Increased Levels of H2-Ea-Specific DNA Breaks in Testicular Germ Cells (2004) (28)
Detection of human papillomavirus DNA in fine‐needle aspirations of metastatic squamous‐cell carcinoma of the uterine cervix using the polymerase chain reaction (1989) (27)
The absence of a human-specific ribosomal DNA transcription factor leads to nucleolar dominance in mouse greater than human hybrid cells (1984) (23)
Gene-centromere linkage mapping by PCR analysis of individual oocytes. (1992) (22)
Gene hunting without sequencing genomic clones: finding exon boundaries in cDNAs. (1998) (21)
Structure and evolution of human and African ape rDNA pseudogenes. (1983) (21)
Sperm typing allows accurate measurement of the recombination fraction between D3S2 and D3S3 on the short arm of human chromosome 3. (1992) (20)
The Mutation Process of Microsatellites During the Polymerase Chain Reaction (2003) (20)
Mitochondrial DNA polymorphism: evidence that variants detected by restriction enzymes differ in nucleotide sequence rather than in methylation. (1980) (19)
High-resolution gametic map of the sheep callipyge region: linkage heterogeneity among rams detected by sperm typing. (1999) (19)
An Inconsistency between Protein Resemblance and Taxonomic Resemblance: Immunological Comparison of Diverse Proteins from Gallinaceous Birds (1975) (18)
Enzymatic Amplification of P-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia (2008) (18)
French Machado-Joseph disease patients do not exhibit gametic segregation distortion: a sperm typing analysis. (1999) (16)
Combining Sperm Typing and Linkage Disequilibrium Analyses Reveals Differences in Selective Pressures or Recombination Rates Across Human Populations (2007) (15)
Evidence for the lack of mismatch-repair directed antirecombination during mouse meiosis. (2002) (14)
The Evolution of Proteins (1973) (14)
Product length, dye choice, and detection chemistry in the bead-emulsion amplification of millions of single DNA molecules in parallel. (2009) (14)
Eliminating primers from completed polymerase chain reactions with exonuclease VII. (1991) (14)
Genetic mapping by single sperm typing. (2009) (13)
Four PCR-based polymorphisms in the pseudoautosomal region of the human X and Y chromosomes. (1993) (12)
Biochemical characterization of “LAP,” a polymorphic aminopeptidase from the blue mussel, Mytilus edulis (1979) (12)
Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region. (1998) (12)
The regional effects of two mutants in Drosophila analyzed by means of mosaics. (1967) (11)
Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typing. (2000) (11)
Studies on the nature and germ-line stability of DNA sequences flanking the mouse immunoglobulin heavy-chain constant-region genes. (1981) (11)
Estimating Exceptionally Rare Germline and Somatic Mutation Frequencies via Next Generation Sequencing (2016) (11)
Single‐Sperm Typing (2002) (10)
Single-molecule analysis of the hypermutable tetranucleotide repeat locus D21S1245 through sperm genotyping: a heterogeneous pattern of mutation but no clear male age effect. (2003) (10)
Analysis of Genetic Data from the Polymerase Chain Reaction (1994) (10)
The mutation properties of spinal and bulbar muscular atrophy disease alleles (1998) (9)
Age dependence of the locations of x-ray induced somatic crossing over in Drosophila. (1966) (9)
Molecular Size of Hagfish Muscle Lactate Dehydrogenase (1967) (9)
[8] Quantitative PCR: Analysis of rare mitochondrial DNA mutations in central nervous system tissues (1995) (8)
Mitochondrial DNA deletions are rare in the free radical-rich retinal environment (1996) (8)
The possible role of Z DNA in chromosomal translocations. (1990) (7)
A New Approach to Constructing Genetic Maps: PCR Analysis of DNA Sequences in Individual Gametes (1989) (6)
Cloning and identification of the pig ribosomal gene promoter. (1994) (6)
Recombination HotSpotintheHuman1-Globin GeneCluster: Meiotic Recombination ofHumanDNA Fragments in Saccharomyces cerevisiae (1985) (6)
14 – Multiple Genes for Lysozyme* (1974) (6)
Direct estimation of the recombination frequency between the RB1 gene and two closely linked microsatellites using sperm typing (1999) (5)
Nuclear magnetic resonance and ultraviolet difference spectral studies of the binding properties of turkey egg white lysozyme. Consequences of the replacement of Asp 101 by glycine. (1974) (4)
Preimplantation genetic diagnosis--a rolling stone gathers no moss! (1992) (4)
The mouse Eb meiotic recombination hotspot contains a tissue-specific transcriptional enhancer (2004) (4)
Combining Data from Polymerase Chain Reaction DNA Typing Experiments: Applications to Sperm Typing Data (1999) (3)
Single-sperm typing : Determination of genetic distance between the Gv . globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers ( genetic recombination / linkage ) (3)
Genetic happing and preimplantation diagnosis in agriculturally important species using single cell PCR (1992) (3)
Genetic recombination analysis using sperm typing. (1994) (3)
Analysis of DNA sequences in individual gametes: application to human genetic mapping. (1990) (2)
Genetic analysis by single cell typing (1994) (2)
THE EVOLUTION OF REGULATORY MECHANISMS STUDIES ON THE MULTIPLE GENES FOR LYSOZYME (1975) (2)
Commercial uses of recombinant DNA technology in human genetic disease. (1988) (2)
7 – Preliminary Biochemical Studies of the Lysozymes of the Black Swan, Cygnus atratus * (1974) (2)
Methods for cloning the vector with a specific nucleic acid sequence contained in a nucleic acid, and for synthesizing a nucleic acid fragment from an existing nucleic acid fragment (1995) (1)
A small molecule in hagfish tissues, possibly related to the cardiac agent, eptatretin. (1968) (1)
The roles of mutation rate and selective pressure on observed levels of the human mitochondrial DNA deletion $\rm mtDNA\sp 4977$ (2003) (1)
The evolutionarily conserved repetitive sequence d(TG.AC)n promotes reciprocal exchange and generates unusual recombinant tetrads during yeast meiosis (1986) (1)
New technologies for studying human genetic variation. (1988) (1)
Single Sperm PCR Analysis — Implications for Preimplantation Genetic Disease Diagnosis (1991) (1)
Pooling strategies for establishing physical genome maps using FISH (1997) (1)
Detection of meiotic DNA breaks in mouse testicular germ cells. (2009) (0)
A method for multiplying and detecting nucleic acid sequences (1996) (0)
The South African ''Bathing Suit Ichthyosis'' Is a Form of Lamellar Ichthyosis Caused by a Homozygous Missense Mutation, p.R315L, in Transglutaminase 1 (2007) (0)
Kit for multiplying and detecting nucleic acid sequences (2004) (0)
Determination of RFLPs linked to multiple sclerosis susceptibility (1987) (0)
Using PCR in preimplantation genetic disease diagnosis. (1992) (0)
Kit for use in the amplification and detection of nucleic acid sequences (1986) (0)
Dating PCR (1990) (0)
Method for increasing, for the detection and / or for the cloning of nucleic acid sequences of. (1986) (0)
“Combining sperm typing and LD analyses reveals differences in selective pressures or recombination rates across human populations” (2006) (0)
Discussion of the Paper (1994) (0)
THE EVOLUTION OF TRANSCRIPTIONAL CONTROL SIGNALS: COEVOLUTION OF RIBOSOMAL GENE PROMOTER SEQUENCES AND TRANSCRIPTION FACTORS (1986) (0)
Erratum: Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene (1994) (0)
Preparation of specific antisera to Drosophila acid phosphatase without rigorous protein purification (1976) (0)
Studying Germline Genetic Events in Single Individuals (2000) (0)
List of Thesis Papers Papers I-iv Are Available in Appendix 1 Individual Variation in Microsatellite Mutation Rate in Barn Swallows. (manuscript) Summaries of Papers including Discussion.. 26 (0)
Molecular Biology and Classical Histology Paraffin-embedded Thin-Tissue Sections : A Bridge between Analysis of DNA Sequences in Forty-Year-Old Updated Version (2006) (0)
Detection of aneuploidy in sperm of an ataxia telangiectasia patient using three-chromosome fluorescence in situ hybridization (1994) (0)
Microinjection of Ras Oncogene Proteins and Inhibitory Antibodies Specific for the Ras Oncogene Proteins into Living Normal and Transformed-Cells (1985) (0)
Kit for use in the amplification and the detection of nucleic acid. (1986) (0)
Book Review:The Primary Structure of Proteins. Principles and Practices for the Determination of Amino Acid Sequence. Walter A. Schroeder (1969) (0)
Cloning of nucleic acid sequence (1992) (0)
Kit for use in the amplification and the proof of nucleic acid sequences (1986) (0)
Detection of new HLA-DPB1 alleles generated by interallelic gene conversion using PCR amplification of DPB1 second exon sequences from sperm (1994) (0)
Germline selection of PTPN11 (HGNC:9644) variants make a major contribution to both Noonan syndrome's high birth rate and the transmission of sporadic cancer variants resulting in fetal abnormality (2022) (0)
A method for amplifying, detecting and / or cloning nucleic acid sequences of of. (1986) (0)
Gene Hunting without Sequencing Genomis Clones: the "Twenty Questions" game with genes (1997) (0)
The Harvey Lectures.Julius Axelrod (1974) (0)
BriefDefinitive Report DETECTION OF HUMAN PAPILLOMA VIRUS IN PARAFFIN-EMBEDDED TISSUE USING THE POLYMERASE CHAIN REACTION (0)
A method for detecting a nucleic acid sequence, and means for carrying out the method as well as methods for cloning vektormed a specific nucleic acid sequence, respectively for synthesizing nucleic acid fragment AFET (1986) (0)
Methods for amplifying and detecting nucleic acid sequences of (1986) (0)
Frequency of Human Disease Mutations and Spermatogonial Stem Cell Function (2017) (0)
Base Mispair Extension Kinetics BINDING OF AVIAN MYELOBLASTOSIS REVERSE TRANSCRIPTASE BASE PAIR TERMINI* TO MATCHED AND MISMATCHED (2001) (0)
A method for detecting the presence or absence of at least one specific nucleic acid sequence in a sample or for distinguishing between two different nucleic acid sequences in said sample (1986) (0)
Recurrent Germline Mutations in the FGFR2/3 Genes, High Mutation Frequency, Paternal Skewing and Age-Dependence (2011) (0)

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