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Human genetics

Showing results (641-650 of 11,264) with videos related to

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Human Genetics|July 1, 1990
DNA polymorphism of the human complement component C7 gene in familial deficienciesE Coto, E Martínez-Naves, O Domínguez, et al.
Human Genetics|February 1, 1990
Marfan syndrome: exclusion of genetic linkage to five genes coding for connective tissue components in the long arm of chromosome 2K Kainulainen, A Savolainen, A Palotie, et al.
Human Genetics|February 1, 1990
A panel of restriction fragment length polymorphisms for chromosomal band 11p13V Huff, D A Compton, L C Strong, et al.
Human Genetics|February 1, 1990
New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locusF Rousseau, A Vincent, I Oberlé, et al.
Human Genetics|February 1, 1990
Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric regionJ S Wu, K K Kidd
Human Genetics|August 8, 2009
Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping resultsRuslan Dorfman, Weili Li, Lei Sun, et al.
Human Genetics|March 1, 1990
Attempt to calculate the allele frequency distribution of a TaqI RFLP detected by the highly polymorphic probe YNH24P H van Eede, T M Cuypers, G G de Lange
Human Genetics|April 1, 1990
A common Chinese beta-thalassemia mutation found in a Japanese familyY Naritomi, H Nakashima, M Kagimoto, et al.
Human Genetics|April 1, 1990
An NcoI restriction fragment length polymorphism at the human steroid sulphatase gene locusP M van Zandvoort, C A van Bennekom, H H Ropers, et al.
Human Genetics|August 27, 2009
Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35)Kerry K Brown, Jacob A Reiss, Kate Crow, et al.
Pageof 1,127

Showing results (641-650 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|July 1, 1990
DNA polymorphism of the human complement component C7 gene in familial deficienciesE Coto, E Martínez-Naves, O Domínguez, et al.
Human Genetics|February 1, 1990
Marfan syndrome: exclusion of genetic linkage to five genes coding for connective tissue components in the long arm of chromosome 2K Kainulainen, A Savolainen, A Palotie, et al.
Human Genetics|February 1, 1990
A panel of restriction fragment length polymorphisms for chromosomal band 11p13V Huff, D A Compton, L C Strong, et al.
Human Genetics|February 1, 1990
New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locusF Rousseau, A Vincent, I Oberlé, et al.
Human Genetics|February 1, 1990
Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric regionJ S Wu, K K Kidd
Human Genetics|August 8, 2009
Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping resultsRuslan Dorfman, Weili Li, Lei Sun, et al.
Human Genetics|March 1, 1990
Attempt to calculate the allele frequency distribution of a TaqI RFLP detected by the highly polymorphic probe YNH24P H van Eede, T M Cuypers, G G de Lange
Human Genetics|April 1, 1990
A common Chinese beta-thalassemia mutation found in a Japanese familyY Naritomi, H Nakashima, M Kagimoto, et al.
Human Genetics|April 1, 1990
An NcoI restriction fragment length polymorphism at the human steroid sulphatase gene locusP M van Zandvoort, C A van Bennekom, H H Ropers, et al.
Human Genetics|August 27, 2009
Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35)Kerry K Brown, Jacob A Reiss, Kate Crow, et al.
Pageof 1,127