Walter Nance | Academic Influence

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Walter Nance

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PhD Computer Science Stanford University

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Why Is Walter Nance Influential?

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According to Wikipedia, Walter Elmore Nance is Professor and Chair of the Department of Human Genetics of the Virginia Commonwealth University. He is an internationally known expert in hereditary deafness, twin studies and genetic linkage analysis of both continuous and qualitative traits.

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Walter Nance's Published Works

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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 Papers

Newborn hearing screening--a silent revolution. (2006) (1261)
Genetic factors in determining bone mass. (1973) (581)
Education policy and the heritability of educational attainment (2016) (319)
Population genetic studies of retinitis pigmentosa. (1980) (305)
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study. (2003) (296)
Factor VIII and factor IX in a twin population. Evidence for a major effect of ABO locus on factor VIII level. (1985) (272)
Predicting zygosity in Norwegian twin pairs born 1915–1960 (1983) (258)
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities (2005) (249)
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss. (2003) (192)
The prevalence of connexin 26 (GJB2) mutations in the Chinese population (2002) (180)
Bivariate genetic analysis of left ventricular mass and weight in pubertal twins (the Medical College of Virginia twin study). (1991) (163)
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22 (2002) (155)
Familial branchio‐oto‐renal dysplasia: A new addition to the branchial arch syndromes (1976) (148)
Hypo‐Functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype‐phenotype correlation or coincidental polymorphisms? (2009) (140)
Genetic models for the analysis of data from the families of identical twins. (1976) (137)
The genetics of deafness (2004) (129)
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness (2002) (125)
Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss. (2006) (124)
X-linked mixed deafness with congenital fixation of the stapedial footplate and perilymphatic gusher. (1971) (122)
Systemic membrane defect in the proximal muscular dystrophies. (1978) (121)
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population (2005) (119)
A twin study of dental dimension. I. Discordance, asymmetry, and mirror imagery. (1976) (117)
Self-reported periodontal disease in a Virginia twin population. (1993) (114)
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians (2003) (111)
Genetic studies of an acardiac monster: evidence of polar body twinning in man. (1981) (107)
Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands. (2003) (106)
A twin study of dental dimension. II. Independent genetic determinants. (1976) (104)
The occurrence of epilepsy and febrile seizures in Virginian and Norwegian twins (1991) (104)
Lactic Dehydrogenase: Genetic Control in Mana (1963) (100)
Clinical findings in four children with biotinidase deficiency detected through a statewide neonatal screening program. (1985) (96)
Parental determinants of birth weight (1984) (94)
GENETIC TESTS WITH A SEX-LINKED MARKER: GLUCOSE-6-PHOSPHATE DEHYDROGENASE. (1964) (94)
Effects of type of placentation on birthweight and its variability in monozygotic and dizygotic twins. (1979) (89)
Clinical heterogeneity in 80 home-reared children with cri du chat syndrome. (1983) (89)
Genetic Analysis of Anthropometric Measures in 11-Year-Old Twins: The Medical College of Virginia Twin Study (1990) (88)
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians (2001) (82)
Relevance of connexin deafness (DFNB1) to human evolution. (2004) (78)
Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands (2003) (77)
Does Universal Newborn Hearing Screening Identify All Children with GJB2 (Connexin 26) Deafness? Penetrance of GJB2 Deafness (2006) (76)
Early onset periodontitis: A comparison and evaluation of two proposed modes of inheritance (1987) (74)
Congenital X-linked cataract, dental anomalies and brachymetacarpalia. (1974) (73)
Discordant expression of fetal hydantoin syndrome in heteropaternal dizygotic twins. (1982) (72)
Spondylocostal dysostosis associated with anal and urogenital anomalies in a Mennonite sibship. (1981) (71)
Relation between choice of partner and high frequency of connexin-26 deafness (2000) (70)
Branchio‐oto‐renal dysplasia and branchio‐oto dysplasia: Two distinct autosomal dominant disorders (1978) (69)
Neonatal screening for biotinidase deficiency: results of a 1-year pilot study. (1986) (67)
Therapeutic effect of vitamin C. A co-twin control study. (1977) (65)
Hemolytic anemia of necrotic arachnidism. (1961) (65)
Goldenhar complex in discordant monozygotic twins: a case report and review of the literature. (1987) (64)
Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity. (1970) (63)
Genetic Control of Hemoglobin Synthesis. (1963) (62)
TURNER'S SYNDROME, TWINNING, AND AN UNUSUAL VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE. (1964) (61)
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations (1998) (60)
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness (2001) (60)
Stain intensity of human nucleolus organizer region reflects incorporation of uridine into mature ribosomal RNA. (1983) (58)
Do twin Lyons have larger spots? (1990) (55)
Autosomal dominant branchiootorenal dysplasia. (1975) (55)
Dermatoglyphic nomogram for the diagnosis of Down's syndrome. (1970) (55)
A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia. (1980) (54)
Autoimmunity in congenital rubella syndrome. (1984) (54)
The use of genetic data in the prediction of craniofacial dimensions. (1973) (53)
A causal analysis of birth weight in the offspring of monozygotic twins. (1983) (52)
Audiological Features of GJB2 (Connexin 26) Deafness (2005) (51)
Studies of age‐correlated features of cognitive‐behavioral development in children and adolescents with genetic disorders (2007) (50)
Symmelia in one of monozygotic twins. (1971) (48)
Epidemiological Studies on Hearing Impairment with Reference to Genetic Factors in Sichuan, China (2001) (47)
Pycnodysostosis, with a familial chromosome anomaly. (1966) (47)
Apparent influence of marker genotypes on variation in serum cholesterol in monozygotic twins (1981) (46)
Univariate genetic analysis of blood pressure in children (the Medical College of Virginia Twin Study). (1989) (45)
Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes (2009) (44)
Anencephaly and Spina Bifida: a Possible Example of Cytoplasmic Inheritance in Man (1969) (43)
Multivariate analysis of craniofacial measurements in twin and family data. (1974) (43)
Effects of chorion type on variation in cord blood cholesterol of monozygotic twins. (1976) (42)
Nucleolar organizer region variants as a risk factor for Down syndrome. (1985) (42)
A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart. (2008) (42)
Amish albinism: a distinctive autosomal recessive phenotype. (1970) (42)
Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: growth, development, and profiles. (1999) (42)
No decline in assortative mating for educational level (1985) (41)
Genetic analysis of dermatoglyphic patterns in twins. (1975) (41)
Genetics of the low density lipoprotein receptor: (1981) (38)
Clinical variation in Usher's syndrome. (1971) (38)
Hereditary adrenocortical unresponsiveness to ACTH. (1970) (38)
Chromosome polymorphism and twin zygosity. (1977) (38)
Apparent cri-du-chat and "antimongolism" in one patient. (1966) (37)
Linkage relations of the loci for Kell and phenylthiocarbamide taste sensitivity. (1976) (35)
Sampling from a skewed population distribution as exemplified by estimation of the creatine kinase upper reference limit. (1984) (35)
Symposium on sensorineural hearing loss in children: early detection and intervention. Genetic factors in deafness of early life. (1975) (34)
Genetic variance in nonverbal intelligence: data from the kinships of identical twins. (1979) (34)
Multivariate Genetic Analysis of Blood Pressure and Body Size: The Medical College of Virginia Twin Study (1992) (33)
Etiology of unilateral hearing loss in a national hereditary deafness repository. (2012) (33)
Prenatal detection of a familial nuchal bleb simulating encephalocele. (1979) (32)
Social inequality and assortative mating: Cause or consequence? (1987) (31)
Antenatally detected Klinefelter's syndrome in twins. (1984) (30)
Orientation of loci within the human major histocompatibility complex by chromosomal in situ hybridization. (1984) (30)
Evidence for a major gene in familial anencephaly. (1990) (30)
Aphidicolin-inducible common fragile-site expression: results from a population survey of twins. (1992) (29)
Myofascial pain dysfunction (MPD) syndrome in twins. (1980) (29)
Data from kinships of monozygotic twins indicate maternal effects on verbal intelligence (1980) (29)
Age-related language characteristics of children and adolescents with fragile X syndrome. (1999) (28)
Partial E-18 long-arm deletion. (1968) (27)
Evidence for autosomal recessive inheritance of the syndrome of renal tubular acidosis with deafness. (1971) (25)
Aortic stiffness: a new Doppler echocardiographic measure predictive of systolic blood pressure in children. (1988) (25)
Interpretation of LOD scores with a set of marker loci (1984) (25)
Malformations unique to the twinning process. (1981) (24)
Congenital Rubella Syndrome and Diabetes: A Review of Epidemiologic, Genetic, and Immunologic Factors (1985) (24)
Genetic Factors in Deafness of Early Life (1975) (23)
Familial aggregation of congenital dislocation of the hip in a Norwegian population. (1988) (22)
Genetic studies of the offspring of identical twins: a model for the analysis of quantitative inheritance in man. (1974) (21)
Models for the longitudinal genetic analysis of same-age twins: application to HDL cholesterol (1998) (21)
A genetic analysis of taste threshold for phenylthiocarbamide. (1981) (21)
Trisomy 8 syndrome. (1975) (21)
Testing for developmental changes in gene expression on resemblance for quantitative traits in kinships of twins: Application to height, weight, and blood pressure (1986) (21)
Partitioned twin analysis: A power study (1989) (20)
Genetic counseling for the hearing impaired. (1971) (18)
LYMPHOCYTE CAPPING IN DUCHENNE MUSCULAR DYSTROPHY (1979) (18)
Human blood pressure and the ABO blood group system: an apparent association. (1965) (18)
Pulmonary arteriovenous malformations related to Rendu-Osler-Weber syndrome. (1984) (18)
GPSM2 mutations in Chudley–McCullough syndrome (2012) (18)
Does the PI polymorphism alone control alpha-1-antitrypsin expression? (1987) (17)
LACTIC DEHYDROGENASE: GENETIC CONTROL IN MAN. (1963) (17)
The Cincinnati lipid research clinic family study: Analysis of commingling and family resemblance for fasting blood glucose (1984) (17)
Genetic linkage studies in a Negro kindred with Norrie's disease. (1969) (17)
Vitiligo and dysgammaglobulinemia. A case report and family study (1975) (17)
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12 (2005) (16)
Familial hypokalemia associated with renal interstitial fibrosis. (1974) (16)
One X and four hypotheses: response to Lehrke's "A Theory of X-Linkage of Major Intellectual Traits. (1972) (16)
The Clinical and Audiologic Features of Hearing Loss Due to Mitochondrial Mutations (2013) (16)
Status and prospects of research in hereditary deafness. (1973) (16)
The larynx in the cri du chat (cat cry) syndrome. (1968) (16)
The Heritability of Smoking Behaviour in Pregnancy, and the Birth Weights of Offspring of Smoking-discordant Twins (1985) (16)
E ring chromosome with persistent left superior vena cava and hypertrophic subaortic stenosis. (1969) (15)
Genetic studies of ocular albinism in a large Virginia kindred. (1984) (15)
Human cytogenetics: a brief review and presentation of new findings. (1967) (15)
Seroepidemiology of cytomegalovirus and herpes simplex virus in twins and their families. (1988) (15)
Familial unilateral deafness and delayed endolymphatic hydrops (2007) (15)
Familial nephrotic syndrome. (1974) (14)
Classification of albinism in man. (1971) (14)
Analysis of the covariance structure of digital ridge counts in the offspring of monozygotic twins. (1983) (14)
Twinning rates in Virginia: secular trends and the effects of maternal age and parity. (1981) (14)
Phenylketonuria heterozygote detection in families with affected children. (1978) (14)
Fine Mapping of the Human Biotinidase Gene and Haplotype Analysis of Five Common Mutations (1999) (14)
Quinacrine mustard and nucleolar organizer region heteromorphisms in twins. (1981) (12)
Further evidence for close linkage of the Hb-beta and Hb-delta loci in man. (1969) (12)
Blood pressure studies on monozygotic twins and their families. (1978) (12)
Femoral duplication: a case report. (1989) (12)
C autosomal trisomy with mosaicism: a new syndrome? (1970) (12)
Genetic and biochemical evidence for two forms of oculocutaneous albinism in man. (1971) (12)
A recessively inherited chondrodystrophy. (1970) (11)
The human X‐chromosome and the levels of serum immunoglobulin M (1979) (11)
1992 American Society of Human Genetics presidential address: back to the future. (1993) (10)
Genetic linkage analysis of human hemoglobin variants. (1970) (10)
Are reference limits for serum creatine kinase valid in detection of the carrier state for Duchenne muscular dystrophy? (1984) (10)
An automated procedure for measuring biotinidase activity in serum. (1989) (10)
Genetic Epidemiology of Deafness (2002) (10)
Current Concepts Newborn Hearing Screening — A Silent Revolution (2010) (10)
TWINS: AN INTRODUCTION TO GEMELLOLOGY (1959) (10)
Linkage analysis using heterozygote detection in phenylketonuria (1979) (9)
Maternal environment defines blood pressure and its response to troleandomycin in spontaneously hypertensive rats. (1995) (9)
Prediction of carrier status in Duchenne dystrophy by creatine kinase measurement. (1985) (9)
Blood pressure in Norwegian twins. (1981) (9)
The contribution of assays for lymphocyte capping and creatine kinase to detection of the Becker-type dystrophy trait. (1980) (9)
Relevance of the marriages of twins to the causal analysis of nonrandom mating. (1981) (9)
Familial twinning: a case for superfetation in man. (1976) (8)
Univariate Genetic Analysis of Oxygen Transport Regulation in Children: The Medical College of Virginia Twin Study (1993) (8)
Familial studies of monozygotic twinning. (1978) (8)
A new tool in birth defects research: the MZ half-sib model and its extension to grandchildren of identical twins. (1978) (8)
Sampling variances in twin and sibling studies of man. (1974) (7)
Quantitative studies of glucose-6-phosphate dehydrogenase. (1977) (7)
A co-twin control study of the effects of vitamin C. (1978) (7)
Lymphocyte capping in Duchenne muscular dystrophy. (1979) (7)
The larynx in the cri du chat (cat cry) syndrome. (1968) (7)
Nonsyndromic deafness. (1980) (7)
Statistical approaches for the detection of heterozygotes for biotinidase deficiency. (1991) (7)
A search for evidence of hereditary superfetation in man. (1978) (7)
Psychology and methodology (1978) (7)
Anencephaly and spina bifida: an etiologic hypothesis. (1971) (7)
The Principles and Practice of Genetic Counseling (1971) (6)
A study of dietary intake in adult monozygotic twins. (1980) (6)
The monozygotic half-sib model: a tool for epidemiologic research. (1978) (6)
Vitamin C and Growth-Reply (1977) (6)
The effect of perinatal screening in Norway on the magnitude of noninherited risk factors for congenital dislocation of the hip. (1987) (5)
Evidence for genetic factors influencing serum uric acid levels in man. (1978) (5)
Distribution of common eye diseases in the families of Norwegian twins. (1982) (5)
The MZ half-sib design: an approach for the examination of the etiology of congenital malformations. (1980) (5)
Human Reproductive Cloning (2002) (5)
Genetic determinants of dental dimension: a twin study. (1978) (5)
The inheritance of immunoglobulin levels. (1978) (5)
On facial similarity in relatives. (1976) (4)
Education in the genetics of hearing loss: A survey of early hearing detection and intervention programs (2006) (4)
A model for the analysis of mate selection in the marriages of twins: application to data on stature. (1980) (4)
The genetic analysis of profound prelingual deafness. (1980) (4)
Mutations in the melanin pigment system in man resulting in features of oculo cutaneous albinism (1972) (4)
Persistent tachycardia, paroxymal hypertension, and seizures: association with hyperglycinuria, dominantly inherited microphthalmia, and cataracts. (1967) (4)
The role of twin studies in human quantitative genetics. (1979) (4)
RADIATION-INDUCED ABNORMALITIES IN HUMAN DEVELOPMENT. (1967) (4)
Popliteal pterygium syndrome in monozygous twins. (1974) (3)
Abnormal Hemoglobins in Human Populations. A Summary and Interpretation. Frank B. Livingstone. Aldine, Chicago, 1967. 482 pp., illus. $12.50 (1968) (3)
Invited Editorial : Do Twin Lyons Have Larger Spots ? (2006) (3)
Plasma Cholesterol in Newborn Human Twins (1975) (3)
GENETICS AND ORTHOPAEDICS. (1965) (3)
Analysis of serum amino acid levels by the twin study method and comparison with family studies. (1978) (3)
Is Assortative Mating the Cause for the High Frequency of Connexin 26 (Cx 26) Deafness? (2000) (3)
The relevance of twin studies to cardiovascular research. (1984) (3)
The analysis of spontaneous abortion using a new half-sib model for qualitative traits. (1981) (2)
Adaptation to maximal effort: genetics vs. environment. A case history. (1984) (2)
Dominantly Inherited Amyotrophic Lateral Sclerosis (Motor Neuron Disease) (1977) (2)
Protecting the privacy of family members in research. (2001) (2)
Dermatoglyphic heterogeneity in mongolis with congenital heart disease. (1973) (2)
Recent developments in genetics: control genes and the genetic code. (1967) (2)
A semiautomated assay procedure for the determination of aminoacyl--tRNA synthetase activity. (1977) (2)
Summary of the Workshop on New Approaches in Twin Research: Applications in Genetic Epidemiology (1987) (2)
A genetic study of erythrocyte arginine-tRNA synthetase activity in man. (1977) (2)
Further comments on the genetics of prelingual deafness. (1989) (2)
Genetic analysis of continuous qualitative and multivariate traits in the families of twins. (1982) (2)
875 BIOTINIDASE DEFICIENCY DETECTED BY A STATEWIDE NEONATAL SCREENING PROGRAM (1985) (1)
Combined pedigree and twin family study to determine the sources of variation in serum biotinidase activity: the usefulness of multiple study designs. (1993) (1)
Effects ofChorion Typeon Variation inCordBlood Cholesterol ofMonozygotic Twins (1976) (1)
The influence of secular effects and gravidity on the rate of ectopic pregnancy in a Norwegian population. (1987) (1)
A note on assortative mating and maternal effects. (1979) (1)
Twin research. Proceedings of the Second International Congress on Twin Studies August 29--September 1, 1977, Washington, DC. Part B. Biology and epidemiology. (1978) (1)
Letter: Note on the analysis of twin data. (1976) (1)
The use of twins in clinical research. (1977) (1)
Inheritance of idiopathic nephrotic syndrome. (1974) (1)
Familial Twinning: A Possible Example of Superfetation In Man (1974) (1)
A Co-twin Control Study of Effect of Vitamin C (1978) (1)
Human Blood and Serum Groups. Otto Prokop and Gerhard Uhlenbruck. Translated from the second German edition (Leipzig, 1966) by John L. Raven. Interscience (Wiley), New York, 1969. xvi + 892 pp., illus. $45 (1970) (1)
The haptoglobin groups in man (1970) (1)
Determinants of ridge counts in MZ twin kinships. (1981) (1)
Genetic and metabolic deafness. By B. W. Konigsmark, M.D., and R. J. Gorlin, D.D.S.,M.S. Philadelphia: W. B. Saunders, 1976, $34.50 (1979) (1)
Common fragile site expression in lymphocytes from an individual mosaic for trisomy 8. (1993) (1)
Reply to López-Bigas et al. (2000) (0)
In encephaloceles, autopsy holds key to genetic counseling: case reports. (1987) (0)
The Relevance of Genetics to Medicine [Introduction] (1977) (0)
Genetic Markers in Human Blood. Eloise R. Giblett. Davis, Philadelphia, 1969. xxviii + 632 pp. + plates. $15 (1970) (0)
A New Form of Hereditary Cerebral Sclerosis (1969) (0)
DOES CENTRAL FAT DEPOSITION (CF) DETERMINE SBP: MCV HEART STUDY (1987) (0)
New Approaches to the Use of Twins in Biomedical Research (1977) (0)
763 THE CURRICULARIZATION OF McKUSICK: AN INNOVATION IN MEDICAL EDUCATION (1985) (0)
Factor VIIIandFactor IXinaTwinPopulation. Evidence foraMajorEffect ofABO LocusonFactor VIIILevel (1985) (0)
Studies of Hereditary Deafness: Present, Past, and Future. (1976) (0)
Editorial help (2004) (0)
Robin M Winter (2004) (0)
Goldenhar syndrome in discordant monozygotic twins an argument against placental vascular anastomoses hypothesis (1986) (0)
DERMATOGLYPHIC HETEROGENEITY IN MONGOLS WITH CONGENITAL HEART DISEASE (2006) (0)
The Genetic Counseling Program at MCV (1977) (0)
VAN DER DOES FRE ARWERT RUNE FRANTS HANS JOENJE BERTUS KUYT MEILAN KWEE CAROLINE de LINT KAMLESH MADAN FRED MENKO JAN (2016) (0)
Affect of late-onset prenatal care on antenatal diagnosis. (1986) (0)
The Hemoglobinopathies: Abnormal Hemoglobins in Human Populations . A Summary and Interpretation. Frank B. Livingstone. Aldine, Chicago, 1967. 482 pp., illus. $12.50. (1968) (0)
WAARDENBURG SYNDROME IS CAUSED BY DEFECTS AT MULTIPLE LOCI, ONE OF WHICH IS TIGHTLY LINKED TO ALPP ON CHROMOSOME-2 - 1ST REPORT OF THE WS CONSORTIUM (1991) (0)
The journal of investigative dermatology: Special issue on cutaneous genetics (1975) (0)
Your Heredity and Environment (2015) (0)
Variability in anthropometric traits in twins and their families. (1988) (0)
Twin research 3. Proceedings of the Third International Congress on Twin Studies. June 16-20, 1980, Jerusalem. Part B Intelligence, personality, and development. (1981) (0)
Caring for children with syndromic features (2005) (0)
Diagnosis of Twin-Zygosity by Dermatoglyphics-Reply (1977) (0)
1044 DISTRIBUTION OF ANTIBODY AGAINST CYTOMEGALOVIRUS (CMV) IN THE FAMILIES OF TWINS (1985) (0)
Genetic Studies of Deafness and of Retinitis Pigmentosa (1977) (0)
POSTER SYMPOSIUM - CEREBRAL BLOOD FLOW (1985) (0)
Medical Genetic Studies in the Amish : Historical Perspective (2003) (0)
A Causal Analysis ofBirth Weight intheOffspring ofMonozygotic Twins (1983) (0)
Biology and epidemiology (1978) (0)
Turner's Syndrome, Twining, and an Unusual Variant of Glucose-6Phosphate Dehydrogenase (2007) (0)
The genetics of gastro-intestinal disorders (1968) (0)
Molecular Screening for Children With Hearing Loss: Why Do It? (2007) (0)
Reviewer Acknowledgment (2013) (0)
515 THE INHERITANCE OF HDL2 CHOLESTEROL AND ITS POSSIBLE ROLE IN CORONARY HEART DISEASE (1985) (0)
Genetic and Enviromental Relationships with the Relative Amount of Plasma Cholesteryl Esters in Children (1978) (0)
Candidate regions for Waardenburg syndrome type II: Search for a second WS locus (1994) (0)
Mutation analysis of USH genes in patients with USH and non-syndromic RP (2002) (0)
1A SYMPOSIUM: INCIDENCE AND FACTORS OF TWINNING THE PROBABLE EXPLANATION FOR THE FALLING TWINNING RATE IN SCOTLAND (2014) (0)
A "new" form of hereditary cerebral sclerosis. An autosomal recessive neurologic disease with distinctive electron electron microscopic findings. (1969) (0)
Traits of Mitochondrial Deafness in a National Repository (2012) (0)
Biochemistry of Human Genetics (1960) (0)
Anatomic studies in the 18-trisomy syndorome . The unusual skeletal findings of the Kuskokwin syndrome . A recessively inherited chondrodystrophy (1970) (0)
International Congress on Twin Studies (2016) (0)
Progress in Medical Genetics (1968) (0)

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