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Human genetics

Showing results (861-870 of 9,569) with videos related to

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Human Genetics|March 1, 1997
Human orosomucoid polymorphism: molecular basis of the three common ORM1 alleles, ORM1*F1, ORM1*F2, and ORM1*SI Yuasa, K Umetsu, U Vogt, et al.
Human Genetics|March 1, 1997
Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35,142 sperm nuclei from two 47,XYY malesE Chevret, S Rousseaux, M Monteil, et al.
Human Genetics|February 1, 1995
Common CFTR mutations are not likely to predispose to chronic bronchitis in northern GermanyA Artlich, A Boysen, S Bunge, et al.
Human Genetics|April 1, 1995
Exclusion of the 13-kDa rapamycin binding protein gene (FKBP2) as a candidate gene for multiple endocrine neoplasia type 1S Grimmond, G Weber, C Larsson, et al.
Human Genetics|September 1, 1995
Mutation analysis of ten exons of the CFTR gene in Greek cystic fibrosis patients: characterization of 74.5% of CF alleles including one novel mutationE Kanavakis, M Tzetis, T Antoniadi, et al.
Human Genetics|July 1, 1994
The polymorphism of the plasma inter-alpha-trypsin inhibitor (ITI) and its relationship to the heavy chain H1 subunit gene (ITIH1) at 3p211-212U Vogt, R Sesboüé, J Bourguignon, et al.
Human Genetics|September 1, 1994
Skipping of multiple CFTR exons is not a result of single exon omissionsA Rickers, F Rininsland, L Osborne, et al.
Human Genetics|October 1, 1995
Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant geneK Kainulainen, H Swan, H Miettinen, et al.
Human Genetics|October 1, 1995
Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU familiesL Kozák, V Kuhrová, M Blazková, et al.
Human Genetics|October 1, 1995
Role of genetic factors in bronchial cancer. Based upon a case of anaplastic lung carcinoma in identical twinsJ M Nores, J F Dalayeun, J Chebat, et al.
Pageof 957

Showing results (861-870 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|March 1, 1997
Human orosomucoid polymorphism: molecular basis of the three common ORM1 alleles, ORM1*F1, ORM1*F2, and ORM1*SI Yuasa, K Umetsu, U Vogt, et al.
Human Genetics|March 1, 1997
Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35,142 sperm nuclei from two 47,XYY malesE Chevret, S Rousseaux, M Monteil, et al.
Human Genetics|February 1, 1995
Common CFTR mutations are not likely to predispose to chronic bronchitis in northern GermanyA Artlich, A Boysen, S Bunge, et al.
Human Genetics|April 1, 1995
Exclusion of the 13-kDa rapamycin binding protein gene (FKBP2) as a candidate gene for multiple endocrine neoplasia type 1S Grimmond, G Weber, C Larsson, et al.
Human Genetics|September 1, 1995
Mutation analysis of ten exons of the CFTR gene in Greek cystic fibrosis patients: characterization of 74.5% of CF alleles including one novel mutationE Kanavakis, M Tzetis, T Antoniadi, et al.
Human Genetics|July 1, 1994
The polymorphism of the plasma inter-alpha-trypsin inhibitor (ITI) and its relationship to the heavy chain H1 subunit gene (ITIH1) at 3p211-212U Vogt, R Sesboüé, J Bourguignon, et al.
Human Genetics|September 1, 1994
Skipping of multiple CFTR exons is not a result of single exon omissionsA Rickers, F Rininsland, L Osborne, et al.
Human Genetics|October 1, 1995
Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant geneK Kainulainen, H Swan, H Miettinen, et al.
Human Genetics|October 1, 1995
Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU familiesL Kozák, V Kuhrová, M Blazková, et al.
Human Genetics|October 1, 1995
Role of genetic factors in bronchial cancer. Based upon a case of anaplastic lung carcinoma in identical twinsJ M Nores, J F Dalayeun, J Chebat, et al.
Pageof 957