Showing results (221-230 of 6,483) with videos related to
Sort By:
Pageof 649
Journal of Medical Genetics|July 1, 1992
Prevalence of congenital anomaly syndromes in a Spanish gypsy populationM L Martínez-Frías, E BermejoJournal of Medical Genetics|February 1, 1997
Genotype-phenotype relationship in 12 patients carrying cystic fibrosis mutation R334WG Antiñolo, S Borrego, M Gili, et al.Journal of Medical Genetics|February 1, 1997
Exclusion of CAG repeat expansion as the cause of disease in autosomal dominant retinitis pigmentosa familiesT J Keen, A G Morris, C F InglehearnJournal of Medical Genetics|February 1, 1997
Functional Xp disomy and de novo t(X;13)(q10;q10) in a girl with hypomelanosis of ItoL S Correa-Cerro, H Rivera, A I VasquezJournal of Medical Genetics|December 1, 1996
Cancer families: what risks are they given and do the risks affect management?E M Rosser, J A Hurst, C J ChapmanJournal of Medical Genetics|December 1, 1996
Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosisT Kubota, S Aradhya, M Macha, et al.Journal of Medical Genetics|December 1, 1996
Identification of carriers of Duchenne/Becker muscular dystrophy by a novel method based on detection of junction fragments in the dystrophin geneH Yamagishi, S Kato, Y Hiraishi, et al.Journal of Medical Genetics|December 1, 1996
Lay understanding of genetics: a test of a hypothesisM Richards, M PonderJournal of Medical Genetics|December 1, 1996
Exclusion of one pedigree affected by adult onset primary open angle glaucoma from linkage to the juvenile glaucoma locus on chromosome 1q21-q31D Avramopoulos, G Kitsos, E Economou-Petersen, et al.Pageof 649