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Annales De Genetique|January 1, 1986
Panel of twenty-five independent man-rodent hybrids for human genetic marker mappingNguyen Van Cong, D Weil, C Finaz, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 13, 2005
[Microarray CGH: principle and use for constitutional disorders]D Sanlaville, J M Lapierre, A Coquin, et al.Annales De Genetique|January 1, 1989
Regional mapping of the human renin gene to 1q32 by in situ hybridizationO Cohen-Haguenauer, F Soubrier, N Van Cong, et al.American Journal of Medical Genetics|November 29, 2002
Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literatureS Brisset, G Joly, C Ozilou, et al.Prenatal Diagnosis|April 21, 1999
Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literatureL Faivre, N Morichon-Delvallez, G Viot, et al.Annales De Genetique|January 1, 1992
Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new casesM Poissonnier, C Turleau, M Olivier-Martin, et al.Human Genetics|October 1, 1990
Investigation of three patients with the "ring syndrome", including familial transmission of ring 5, and estimation of reproductive risksK D MacDermot, E Jack, A Cooke, et al.American Journal of Human Genetics|December 1, 1991
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndromeH J Lüdecke, C Johnson, M J Wagner, et al.Human Reproduction (Oxford, England)|February 3, 2007
Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case reportValérie Malan, R Gesny, N Morichon-Delvallez, et al.Human Reproduction (Oxford, England)|January 5, 2001
Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and menJ Gekas, F Thepot, C Turleau, et al.Pageof 17