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Human genetics

Showing results (901-910 of 9,569) with videos related to

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Human Genetics|April 7, 1977
Bf polymorphism: another variant (S0.8)G Hauptmann, E Wertheimer, M M Tongio, et al.
Human Genetics|April 15, 1977
Erythrocyte superoxide dismutase in different racial groups in Malaysia. A variant in a FilipinoY S Teng, L E Lie-Ingo
Human Genetics|April 15, 1977
Autosomal recessive microcephaly associated with chorioretinopathyJ M Cantú, J A Rojas, D García-Cruz, et al.
Human Genetics|September 1, 1996
beta-Glucuronidase P408S, P415L mutations: evidence that both mutations combine to produce an MPS VII allele in certain Mexican patientsM R Islam, R Vervoort, W Lissens, et al.
Human Genetics|September 1, 1996
Polymorphisms of apolipoproteins A-IV and E in a Turkish population living in GermanyE Malle, K P Pfeiffer, K Dugi, et al.
Human Genetics|September 1, 1996
Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populationsH G de Vries, M A van der Meulen, R Rozen, et al.
Human Genetics|September 1, 1996
Heteroduplex and protein truncation analysis of the BRCA1 185delAG mutationH Ozcelik, Y J Antebi, D E Cole, et al.
Human Genetics|September 1, 1996
Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involvedI Mammi, D E Iles, D Smeets, et al.
Human Genetics|September 1, 1996
Transcript analysis of CFTR frameshift mutations in lymphocytes using the reverse transcription-polymerase chain reaction technique and the protein truncation testM C Romey, S Tuffery, M Desgeorges, et al.
Human Genetics|September 1, 1996
Identification of a variable number tandem repeat region in the human T cell receptor alpha-delta (TCRAD) locusH Buchmayer, H Rumpold, C Mannhalter
Pageof 957

Showing results (901-910 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|April 7, 1977
Bf polymorphism: another variant (S0.8)G Hauptmann, E Wertheimer, M M Tongio, et al.
Human Genetics|April 15, 1977
Erythrocyte superoxide dismutase in different racial groups in Malaysia. A variant in a FilipinoY S Teng, L E Lie-Ingo
Human Genetics|April 15, 1977
Autosomal recessive microcephaly associated with chorioretinopathyJ M Cantú, J A Rojas, D García-Cruz, et al.
Human Genetics|September 1, 1996
beta-Glucuronidase P408S, P415L mutations: evidence that both mutations combine to produce an MPS VII allele in certain Mexican patientsM R Islam, R Vervoort, W Lissens, et al.
Human Genetics|September 1, 1996
Polymorphisms of apolipoproteins A-IV and E in a Turkish population living in GermanyE Malle, K P Pfeiffer, K Dugi, et al.
Human Genetics|September 1, 1996
Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populationsH G de Vries, M A van der Meulen, R Rozen, et al.
Human Genetics|September 1, 1996
Heteroduplex and protein truncation analysis of the BRCA1 185delAG mutationH Ozcelik, Y J Antebi, D E Cole, et al.
Human Genetics|September 1, 1996
Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involvedI Mammi, D E Iles, D Smeets, et al.
Human Genetics|September 1, 1996
Transcript analysis of CFTR frameshift mutations in lymphocytes using the reverse transcription-polymerase chain reaction technique and the protein truncation testM C Romey, S Tuffery, M Desgeorges, et al.
Human Genetics|September 1, 1996
Identification of a variable number tandem repeat region in the human T cell receptor alpha-delta (TCRAD) locusH Buchmayer, H Rumpold, C Mannhalter
Pageof 957