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Human genetics

Showing results (401-410 of 11,264) with videos related to

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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.
Human Genetics|July 1, 1995
Mutations in three subdomains of the carboxy-terminal region of collagen type X account for most of the Schmid metaphyseal dysplasiasJ Bonaventure, F Chaminade, P Maroteaux
Human Genetics|July 1, 1995
A 15-base pair (bp) palindromic insertion associated with a 3-bp deletion in exon 10 of the gp91-phox gene, detected in two patients with X-linked chronic granulomatous diseaseT Ariga, Y Sakiyama, S Matsumoto
Human Genetics|July 1, 1995
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutationA F van Lieburg, M A Verdijk, F Schoute, et al.
Human Genetics|July 1, 1995
Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literatureS Demczuk, A Lévy, M Aubry, et al.
Human Genetics|July 1, 1995
Two recurrent nonsense mutations and a 4 bp deletion in a quasi-symmetric element in exon 37 of the NF1 geneP N Robinson, A Böddrich, H Peters, et al.
Human Genetics|July 1, 1995
Human glutamine: fructose-6-phosphate amidotransferase: characterization of mRNA and chromosomal assignment to 2p13J Zhou, J L Neidigh, R Espinosa, et al.
Human Genetics|July 18, 1979
G-banding patterns of high-resolution human chromosomes 6--22, X, and YJ J Yunis, D W Ball, J R Sawyer
Pageof 1,127

Showing results (401-410 of 11,264) with videos related to

Sort By:
Pageof 1,127
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.
Human Genetics|July 1, 1995
Mutations in three subdomains of the carboxy-terminal region of collagen type X account for most of the Schmid metaphyseal dysplasiasJ Bonaventure, F Chaminade, P Maroteaux
Human Genetics|July 1, 1995
A 15-base pair (bp) palindromic insertion associated with a 3-bp deletion in exon 10 of the gp91-phox gene, detected in two patients with X-linked chronic granulomatous diseaseT Ariga, Y Sakiyama, S Matsumoto
Human Genetics|July 1, 1995
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutationA F van Lieburg, M A Verdijk, F Schoute, et al.
Human Genetics|July 1, 1995
Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literatureS Demczuk, A Lévy, M Aubry, et al.
Human Genetics|July 1, 1995
Two recurrent nonsense mutations and a 4 bp deletion in a quasi-symmetric element in exon 37 of the NF1 geneP N Robinson, A Böddrich, H Peters, et al.
Human Genetics|July 1, 1995
Human glutamine: fructose-6-phosphate amidotransferase: characterization of mRNA and chromosomal assignment to 2p13J Zhou, J L Neidigh, R Espinosa, et al.
Human Genetics|July 18, 1979
G-banding patterns of high-resolution human chromosomes 6--22, X, and YJ J Yunis, D W Ball, J R Sawyer
Pageof 1,127