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Human Molecular Genetics|August 1, 1993

Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndromeC Chevillard, D Le Paslier, E Passage, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 22, 2001

Unequal VH gene rearrangement frequency within the large VH7183 gene family is not due to recombination signal sequence variation, and mapping of the genes shows a bias of rearrangement based on chromosomal locationG S Williams, A Martinez, A Montalbano, et al.

Journal of Medical Genetics|July 4, 2001

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the diseaseL Villard, N Lévy, F Xiang, et al.

Journal of Medical Genetics|November 3, 2004

Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertilityN Machev, N Saut, G Longepied, et al.

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Showing results (91-100 of 94) with videos related to

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You have reached the last page of results.This site can display upto 94 results.

Human Molecular Genetics|August 1, 1993

Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndromeC Chevillard, D Le Paslier, E Passage, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 22, 2001

Unequal VH gene rearrangement frequency within the large VH7183 gene family is not due to recombination signal sequence variation, and mapping of the genes shows a bias of rearrangement based on chromosomal locationG S Williams, A Martinez, A Montalbano, et al.

Journal of Medical Genetics|July 4, 2001

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the diseaseL Villard, N Lévy, F Xiang, et al.

Journal of Medical Genetics|November 3, 2004

Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertilityN Machev, N Saut, G Longepied, et al.

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