Showing results (101-110 of 7,005) with videos related to

Sort By:
Pageof 701
American Journal of Human Genetics|November 1, 1990
More than one mutant allele causes infantile Tay-Sachs disease in French-CanadiansP Hechtman, F Kaplan, J Bayleran, et al.
Molecular Human Reproduction|September 28, 2004
Chromosome aneuploidy in the spermatozoa of two men with globozoospermiaF Morel, N Douet-Guilbert, A Moerman, et al.
American Journal of Human Genetics|July 1, 1992
Time and space clusters of the French-Canadian M1V phenylketonuria mutation in FranceS Lyonnet, D Melle, M de Braekeleer, et al.
International Journal of Andrology|January 26, 2008
Increased aneuploidy rates in spermatozoa of a male carrier of a trisomy 18 mosaicismA Perrin, N Douet-Guilbert, M J Le Bris, et al.
Human Reproduction (Oxford, England)|October 26, 2006
Meiotic segregation in spermatozoa of a 45,XY,-14,der(18)t(14;18)(q11;p11.3) translocation carrier: a case reportA Perrin, N Douet-Guilbert, B Laudier, et al.
American Journal of Human Genetics|August 1, 1993
A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of QuebecF Merante, R Petrova-Benedict, N MacKay, et al.
Annales De Genetique|January 1, 1992
Genetic epidemiology of lipoprotein lipase deficiency in Saguenay-Lac-St-Jean (Québec, Canada)C Dionne, C Gagné, P Julien, et al.
Pageof 701