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Clinical Genetics|November 1, 1993
Cranial hemihypertrophy with ipsilateral naevoid streaks, intellectual handicap and epilepsy: a report of two casesG P McMullin, M Super, M A ClarkeClinical Genetics|November 1, 1993
Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversionJ G Wauters, P J Bossuyt, L Roelen, et al.Clinical Genetics|February 1, 1995
Impact of a common mutation of the LDL receptor gene, in French-Canadian patients with familial hypercholesterolemia, on means, variances and correlations among traits of lipid metabolismM Roy, C F Sing, C Betard, et al.Clinical Genetics|May 1, 1993
Chromosome painting using FISH (fluorescence in situ hybridization) with chromosome-6-specific library demonstrates the origin of a de novo 6q+ marker chromosomeK Brøndum-Nielsen, S Bajalica, K Wulff, et al.Clinical Genetics|May 1, 1993
Germinal mosaicism in a Duchenne muscular dystrophy family: implications for genetic counsellingM A Melis, M Cau, R Congiu, et al.Clinical Genetics|February 1, 1977
Morphology of the placenta in fetal I-cell diseaseJ Rapola, P AulaClinical Genetics|February 1, 1977
Adrenoleukodystrophy (Siemerling-creutzfeldt disease): Heterozygote with two clonal fibroblast populationsH H Ropers, J Zimmermann, T WienkerClinical Genetics|February 1, 1977
A case of double trisomy in a liveborn infant: 48, XXY, "13J B Malhes, C M Moore, J J GershankClinical Genetics|February 1, 1977
Cystic fibrosis: Evidence for a genetic compound from a family study in cell cultureB S Danes, M E Hodson, J BattenClinical Genetics|February 1, 1977
Two XX males in one family and additional observations bearing on the etiology of XX malesA D Chapelle, J Schröder, J Murros, et al.Pageof 718