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Journal of Medical Genetics|January 1, 1997
Maternal uniparental disomy 7 in Silver-Russell syndromeM A Preece, S M Price, V Davies, et al.Journal of Medical Genetics|January 1, 1997
46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosisC P Venditti, N K Seese, G S Gerhard, et al.Journal of Medical Genetics|January 1, 1997
Metacarpophalangeal pattern (MCPP) profile analysis in a family with triphalangeal thumbJ Zguricas, P F Dijkstra, E S Gelsema, et al.Journal of Medical Genetics|January 1, 1997
Preparing for presymptomatic DNA testing for early onset Alzheimer's disease/cerebral haemorrhage and hereditary Pick diseaseA Tibben, M Stevens, G M de Wert, et al.Journal of Medical Genetics|January 1, 1997
Fortuitous detection of uniparental isodisomy of chromosome 6M C Bittencourt, M A Morris, J Chabod, et al.Journal of Medical Genetics|January 1, 1997
Anal anomalies: an uncommon feature of velocardiofacial (Shprintzen) syndrome?S Worthington, A Colley, K Fagan, et al.Journal of Medical Genetics|December 1, 1996
Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25A Raas-Rothschild, S Manouvrier, M Gonzales, et al.Journal of Medical Genetics|December 1, 1996
The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 yearsC Tysoe, D Robinson, C Brayne, et al.Journal of Medical Genetics|December 1, 1996
Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X familyB B de Vries, C C Jansen, A A Duits, et al.Journal of Medical Genetics|December 1, 1996
Unexpected HLA haplotype sharing in dizygotic twin pairs discordant for rheumatoid arthritisD Jawaheer, A J MacGregor, P K Gregersen, et al.Pageof 649