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The Journal of Pediatrics|July 1, 1996
Isolated X-linked thrombocytopenia in two unrelated families is associated with point mutations in the Wiskott-Aldrich syndrome protein geneG de Saint Basile, R D Lagelouse, N Lambert, et al.Molecular Human Reproduction|December 2, 2000
Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutationsP Jézéquel, C Dubourg, D Le Lannou, et al.Prenatal Diagnosis|October 12, 2010
Pediatric outcome of children with the prenatal diagnosis of isolated septal agenesisL Damaj, B Bruneau, M Ferry, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1994
[Reflections on 10 years of medically induced abortions in Ille-et-Vilaine]S Schneider, M Roussey, S Odent, et al.Gynecologie, Obstetrique & Fertilite|June 27, 2015
[Reproductive health care for women with spina bifida]D Body-Bechou, A-S Cabaret-Dufour, L Siproudhis, et al.Molecular Syndromology|February 20, 2014
Currarino Syndrome and HPE Microform Associated with a 2.7-Mb Deletion in 7q36.3 Excluding SHH GeneC Coutton, B Poreau, F Devillard, et al.American Journal of Medical Genetics|March 3, 1998
Central nervous system malformations and early end-stage renal disease in oro-facio-digital syndrome type I: a reviewS Odent, B Le Marec, A Toutain, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1989
[Indications for therapeutic interruption of pregnancy in Ille-et-Villaine from 1982 to 1986. Apropos of 222 cases]M Roussey, B Libeau, B Le Marec, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|May 18, 1994
Remarks about the prognosis in case of antenatal diagnosis of gastroschisisP Poulain, J Milon, B Frémont, et al.Human Genetics|April 1, 1993
Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20I Dorval, S Odent, P Jezequel, et al.Pageof 11