Relation between choice of partner and high frequency of connexin-26 deafnessNANCE, W. E; LIU, X.-Z; PANDYA, A et al.Lancet (British edition). 2000, Vol 356, Num 9228, pp 500-501, issn 0140-6736Article

Seroepidemiology of cytomegalovirus and herpes simplex virus in twins and their familiesBODURTHA, J; ADLER, S. P; NANCE, W. E et al.American journal of epidemiology. 1988, Vol 128, Num 2, pp 268-276, issn 0002-9262Article

The effect of perinatal screening in Norway on the magnitude of nonherited risk factors for congenital dislocation of the hipKRAMER, A. A; BERG, K; NANCE, W. E et al.American journal of epidemiology. 1987, Vol 125, Num 2, pp 271-276, issn 0002-9262Article

Predicting zygosity in Norwegian twin pairs born 1915-1960MAGNUS, P; BERG, K; NANCE, W. E et al.Clinical genetics. 1983, Vol 24, Num 2, pp 103-112, issn 0009-9163Article

Goldenhar complex in discordant monozygotic twins: a case reort and review of the literatureBOLES, D. J; BODURTHA, J; NANCE, W. E et al.American journal of medical genetics. 1987, Vol 28, Num 1, pp 103-109, issn 0148-7299Article

Pulmonary arteriovenous malformations related to Rendu-Osler-Weber syndromeMCCUE, C. M; HARTENBERG, M; NANCE, W. E et al.American journal of medical genetics. 1984, Vol 19, Num 1, pp 19-27, issn 0148-7299Article

Waardenburg syndrome type 3 (Klein-Waardenburg syndrome) segregating with a heterozygous deletion in the paired box domain of PAX3: a simple variant or a true syndrome?TEKIN, M; BODURTHA, J. N; NANCE, W. E et al.Clinical genetics. 2001, Vol 60, Num 4, pp 301-304, issn 0009-9163Article

Parental determinants of birth weightMAGNUS, P; BERG, K; BJERKEDAL, T et al.Clinical genetics. 1984, Vol 26, Num 5, pp 397-405, issn 0009-9163Article

Congenital rubella syndrome and diabetes: a review of epidemiologic, genetic, and immunologic factorsSHAVER, K. A; BOUGHMAN, J. A; NANCE, W. E et al.American annals of the deaf (Washington, DC. 1886). 1985, Vol 130, Num 6, pp 526-532, issn 0002-726XArticle

The heritability of smoking behaviour in pregnancy, and the birth weights of offspring of smoking-discordant twinsMAGNUS, P; BERG, K; BJERKEDAL, T et al.Scandinavian journal of social medicine. 1985, Vol 13, Num 1, pp 29-34, issn 0300-8037Article

High-density lipoprotein-cholesterol subfractions in adolescent twinsBODURTHA, J. N; SCHIEKEN, R; SEGREST, J et al.Pediatrics (Evanston). 1987, Vol 79, Num 2, pp 181-189, issn 0031-4005Article

A novel deletion involving the connexin-30 gene, del(GJb6-d13s1854), found in frans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairmentDEL CASTILLO, F. J; RODRIGUEZ-BALLESTEROS, M; PANDYA, A et al.Journal of medical genetics. 2005, Vol 42, Num 7, pp 588-594, issn 0022-2593, 7 p.Article

Attitudes of deaf and hard of hearing subjects towards genetic testing and prenatal diagnosis of hearing lossSTERN, S. J; ARNOS, K. S; MURRELLE, L et al.Journal of medical genetics. 2002, Vol 39, Num 6, pp 449-453, issn 0022-2593Article

Linkage studies in a large kindred with hereditary pancreatitis confirms mapping of the gene to a 16-cM region on 7qPANDYA, A; HALLORAN BLANTON, S; LANDA, B et al.Genomics (San Diego, Calif.). 1996, Vol 38, Num 2, pp 227-230, issn 0888-7543Article

Analysis of locus heterogeneity in Waardenburg syndrome types 1 and 2 using highly informative microsatellite markersREYNOLDS, J. E; ARNOS, K. S; MACLEAN, C et al.Human heredity. 1995, Vol 45, Num 5, pp 243-252, issn 0001-5652Article

Analysis of variability of clinical manifestations in Waardenburg syndromeREYNOLDS, J. E; MEYER, J. M; LANDA, B et al.American journal of medical genetics. 1995, Vol 57, Num 4, pp 540-547, issn 0148-7299Article

Common fragile site expression in lymphocytes from an individual mosaic for trisomy 8AUSTIN, M. J. F; NEALE, M. C; COREY, L. A et al.American journal of medical genetics. 1993, Vol 45, Num 5, pp 570-571, issn 0148-7299Article

Aphidicolin-inducible common fragile-site expression : results from a population survey of twinsAUSTIN, M. J. F; COLLINS, J. M; COREY, L. A et al.American journal of human genetics. 1992, Vol 50, Num 1, pp 76-83, issn 0002-9297Article

Evidence for a major gene in familial anencephalySHAFFER, L. G; MARAZITA, M. L; BODURTHA, J et al.American journal of medical genetics. 1990, Vol 36, Num 1, pp 97-101, issn 0148-7299, 5 p.Article

The influence of secular effects and gravidity on the rate of ectopic pregnancy in a Norwegian populationBUCK, G. M; KRAMER, A. A; NANCE, W. E et al.International journal of epidemiology. 1987, Vol 16, Num 3, pp 431-435, issn 0300-5771Article

Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypesCHOI, B. Y; MADEO, A. C; KING, K. A et al.Journal of medical genetics. 2009, Vol 46, Num 12, pp 856-861, issn 0022-2593, 6 p.Article

F emoral duplication: a case reportBODURTHA, J; COUTINHO, M; BENATOR, R et al.American journal of medical genetics. 1989, Vol 33, Num 2, pp 165-169, issn 0148-7299Article

Updating McKusick: an educational exercise for medical studentsBODURTHA, J. N; TOWNSEND, J. I; PROUD, V. K et al.American journal of medical genetics. 1986, Vol 24, Num 3, pp 505-511, issn 0148-7299Article

Neonatal screening for biotinidase deficiency: results of a 1-year pilot studyHEARD, G. S; WOLF, B; JEFFERSON, L. G et al.The Journal of pediatrics. 1986, Vol 108, Num 1, pp 40-46, issn 0022-3476Article

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