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Human Genetics|July 1, 1995
Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 geneE K Bijlsma, P Merel, P Fleury, et al.Human Genetics|July 1, 1995
Absence of mutations in the WT1 gene in patients with XY gonadal dysgenesisA Nordenskjöld, G Fricke, M AnvretHuman Genetics|July 1, 1995
Detection and characterization of new mutations in the human angiotensinogen gene (AGT)J E Hixson, P K PowersHuman Genetics|July 1, 1995
Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literatureC M Tuck-Muller, H Chen, J E Martínez, et al.Human Genetics|July 1, 1995
Detection of a CfoI polymorphism within exon 5 of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit gene (CHRNA4)O SteinleinHuman Genetics|July 1, 1995
Transferable clastogenic activity in plasma from patients with Fanconi anemiaI Emerit, A Levy, G Pagano, et al.Human Genetics|July 1, 1995
Evidence for a cholesterol-lowering gene in a French-Canadian kindred with familial hypercholesterolemiaC Sass, L M Giroux, Y Ma, et al.Human Genetics|July 1, 1995
Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36H Eiberg, A M Lund, M Warburg, et al.Human Genetics|July 1, 1995
The X-chromosomal human biglycan gene BGN is subject to X inactivation but is transcribed like an X-Y homologous geneC Geerkens, U Vetter, W Just, et al.Human Genetics|July 1, 1995
Maternal origin of nucleated erythrocytes in peripheral venous blood of pregnant womenA Slunga-Tallberg, W el-Rifai, M Keinänen, et al.Pageof 959