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Human genetics

Showing results (501-510 of 11,264) with videos related to

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Human Genetics|March 1, 1993
Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigreeA Sander, H Moser, S Liechti-Gallati, et al.
Human Genetics|March 1, 1993
Four separate regions on chromosome 17 show loss of heterozygosity in familial breast carcinomasA Lindblom, L Skoog, T I Andersen, et al.
Human Genetics|March 1, 1993
D21S210: a highly polymorphic (GT)n marker closely linked to the beta-amyloid protein precursor (APP) geneA C Warren, M G McInnis, M Kalaitsidaki, et al.
Human Genetics|January 1, 1980
Gd(-) Rennes, a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia found in FranceC Picat, J Etiemble, P Boivin, et al.
Human Genetics|January 1, 1980
A new approach in the evaluation of chromosome variants in man. II. Pairs without Q or C (qh) variantsJ Azumi, Y Nakagome, S Oka, et al.
Human Genetics|January 1, 1980
A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family membersA Smith, M Noel
Human Genetics|January 1, 1980
Diaphragmatic defects in children of consanguineous parentsI Arad, G C Lijovetzky, R Starinsky, et al.
Human Genetics|January 1, 1980
Chromosome studies on lymphocytes of patients under cytostatic therapy. II. Studies Using the BUDR-labelling technique in cytostatic interval therapyE Gebhart, B Windolph, F Wopfner
Human Genetics|January 1, 1980
Abnormal cerebral cortical convolutions in an XYY fetusG E Austin, R S Sparkes
Human Genetics|January 1, 1980
H-Y antigen in X,i(Xq) gonadal dysgenesis: evidence of X-linked genes in testicular differentiationS S Wachtel, G C Koo, W R Breg, et al.
Pageof 1,127

Showing results (501-510 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|March 1, 1993
Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigreeA Sander, H Moser, S Liechti-Gallati, et al.
Human Genetics|March 1, 1993
Four separate regions on chromosome 17 show loss of heterozygosity in familial breast carcinomasA Lindblom, L Skoog, T I Andersen, et al.
Human Genetics|March 1, 1993
D21S210: a highly polymorphic (GT)n marker closely linked to the beta-amyloid protein precursor (APP) geneA C Warren, M G McInnis, M Kalaitsidaki, et al.
Human Genetics|January 1, 1980
Gd(-) Rennes, a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia found in FranceC Picat, J Etiemble, P Boivin, et al.
Human Genetics|January 1, 1980
A new approach in the evaluation of chromosome variants in man. II. Pairs without Q or C (qh) variantsJ Azumi, Y Nakagome, S Oka, et al.
Human Genetics|January 1, 1980
A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family membersA Smith, M Noel
Human Genetics|January 1, 1980
Diaphragmatic defects in children of consanguineous parentsI Arad, G C Lijovetzky, R Starinsky, et al.
Human Genetics|January 1, 1980
Chromosome studies on lymphocytes of patients under cytostatic therapy. II. Studies Using the BUDR-labelling technique in cytostatic interval therapyE Gebhart, B Windolph, F Wopfner
Human Genetics|January 1, 1980
Abnormal cerebral cortical convolutions in an XYY fetusG E Austin, R S Sparkes
Human Genetics|January 1, 1980
H-Y antigen in X,i(Xq) gonadal dysgenesis: evidence of X-linked genes in testicular differentiationS S Wachtel, G C Koo, W R Breg, et al.
Pageof 1,127