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Human Reproduction (Oxford, England)|August 19, 2006
Meiotic segregation analysis in spermatozoa of pericentric inversion carriers using fluorescence in-situ hybridizationF Morel, B Laudier, F Guérif, et al.American Journal of Human Genetics|October 1, 1990
Cystic fibrosis mutations in North American populations of French ancestry: analysis of Quebec French-Canadian and Louisiana Acadian familiesR Rozen, R H Schwartz, B C Hilman, et al.American Journal of Medical Genetics. Part A|August 23, 2005
Detection of an unexpected subtelomeric 15q26.2 --> qter deletion in a little girl: clinical and cytogenetic studiesL Pinson, A Perrin, C Plouzennec, et al.Human Reproduction (Oxford, England)|August 10, 2004
Lack of intraindividual variation of unbalanced spermatozoa frequencies from a 46,XY,t(9;22)(q21;q11.2) carrier: case reportF Morel, N Douet-Guilbert, M-J Le Bris, et al.Clinical Genetics|April 1, 1992
Prevalence, geographical distribution and genealogical investigations of mutation 188 of lipoprotein lipase gene in the French Canadian population of QuébecJ Bergeron, T Normand, A Bharucha, et al.Human Genetics|August 1, 1992
Geographic distribution and genealogy of mutation 207 of the lipoprotein lipase gene in the French Canadian population of QuébecT Normand, J Bergeron, T Fernandez-Margallo, et al.Human Reproduction (Oxford, England)|November 8, 2007
Segregation of chromosomes in sperm of a t(X;18)(q11;p11.1) carrier inherited from his mother: case reportA Perrin, N Douet-Guilbert, M J Le Bris, et al.Andrologia|March 12, 2014
Balanced complex chromosome rearrangement in male infertility: case report and literature reviewM H Nguyen, F Morel, P Pennamen, et al.Genetic Counseling (Geneva, Switzerland)|March 23, 2007
Prenatal diagnosis of a mosaic 45,X/46,X,r(X)46,XX with a small ring of the X chromosomeM J Le Bris, H Le Guern, C Plouhinec, et al.Annals of Neurology|March 11, 1999
Stroke-like episodes in autosomal recessive cytochrome oxidase deficiencyC Morin, J Dubé, B H Robinson, et al.Pageof 701