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Human genetics

Showing results (81-90 of 11,257) with videos related to

Pageof 1,126
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Human Genetics|August 14, 2001
Improved definition of chromosomal breakpoints using high-resolution multicolour bandingJ Lemke, I Chudoba, G Senger, et al.
Human Genetics|August 2, 2001
Genetic basis of mitochondrial HMG-CoA synthase deficiencyR Aledo, J Zschocke, J Pié, et al.
Human Genetics|August 2, 2001
Niemann-Pick type C disease: NPC1 mutations associated with severe and mild cellular cholesterol trafficking alterationsI Ribeiro, A Marcão, O Amaral, et al.
Human Genetics|August 2, 2001
Frequency of replication/transcription errors in (A)/(T) runs of human genesA Paoloni-Giacobino, C Rossier, M P Papasavvas, et al.
Human Genetics|August 2, 2001
Identification of duplicated genes in 17q11.2 using FISH on stretched chromosomes and DNA fibersA Bentivegna, M Venturin, C Gervasini, et al.
Human Genetics|August 2, 2001
A molecular approach to dominance in hypophosphatasiaA S Lia-Baldini, F Muller, A Taillandier, et al.
Human Genetics|March 1, 1992
Complementation of a DNA repair deficiency in six human tumor cell lines by chromosome 11R Parshad, F M Price, M Oshimura, et al.
Human Genetics|March 1, 1992
PKU mutations R408Q and F299C in Norway: haplotype associations, geographic distributions and phenotype characteristicsH G Eiken, K Stangeland, L Skjelkvåle, et al.
Human Genetics|May 19, 1976
Partial and complete trisomy 9: delineation of a trisomy 9 syndromeG R Sutherland, R F Carter, L L Morris
Human Genetics|May 19, 1976
Increased sister chromatid exchange events in the human late replicating XW Schnedl, W Pumberger, R Czaker, et al.
Pageof 1,126

Showing results (81-90 of 11,257) with videos related to

Sort By:
Pageof 1,126
Human Genetics|August 14, 2001
Improved definition of chromosomal breakpoints using high-resolution multicolour bandingJ Lemke, I Chudoba, G Senger, et al.
Human Genetics|August 2, 2001
Genetic basis of mitochondrial HMG-CoA synthase deficiencyR Aledo, J Zschocke, J Pié, et al.
Human Genetics|August 2, 2001
Niemann-Pick type C disease: NPC1 mutations associated with severe and mild cellular cholesterol trafficking alterationsI Ribeiro, A Marcão, O Amaral, et al.
Human Genetics|August 2, 2001
Frequency of replication/transcription errors in (A)/(T) runs of human genesA Paoloni-Giacobino, C Rossier, M P Papasavvas, et al.
Human Genetics|August 2, 2001
Identification of duplicated genes in 17q11.2 using FISH on stretched chromosomes and DNA fibersA Bentivegna, M Venturin, C Gervasini, et al.
Human Genetics|August 2, 2001
A molecular approach to dominance in hypophosphatasiaA S Lia-Baldini, F Muller, A Taillandier, et al.
Human Genetics|March 1, 1992
Complementation of a DNA repair deficiency in six human tumor cell lines by chromosome 11R Parshad, F M Price, M Oshimura, et al.
Human Genetics|March 1, 1992
PKU mutations R408Q and F299C in Norway: haplotype associations, geographic distributions and phenotype characteristicsH G Eiken, K Stangeland, L Skjelkvåle, et al.
Human Genetics|May 19, 1976
Partial and complete trisomy 9: delineation of a trisomy 9 syndromeG R Sutherland, R F Carter, L L Morris
Human Genetics|May 19, 1976
Increased sister chromatid exchange events in the human late replicating XW Schnedl, W Pumberger, R Czaker, et al.
Pageof 1,126