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American Journal of Medical Genetics. Part A|April 4, 2008
Trisomy 20q caused by interstitial duplication 20q13.2: clinical report and literature reviewPierre Blanc, Laetitia Gouas, Christine Francannet, et al.
Annales De Genetique|March 31, 2004
Genetics of nonsyndromic cleft lip with or without cleft palate: is there a Mendelian sub-entity?Vincent Gajdos, Michel Bahuau, Elisabeth Robert-Gnansia, et al.
Clinical Genetics|April 23, 2023
Discovering the ANK2-related autism phenotypeClaire Guissart, Anne Polge, Nelly Durand, et al.
Gene|June 19, 2013
A new mutation that predicted a drastic alteration of the BTK protein functionAnne Debost-Legrand, Guillaume Legrand, Gaelle Moulillot, et al.
Congenital Anomalies|February 21, 2019
Association between hereditary predisposition to common cancers and congenital multimalformationsFabrice Kwiatkowski, Isabelle Perthus, Nancy Uhrhammer, et al.
BMC Pregnancy and Childbirth|March 25, 2014
False positive morphologic diagnoses at the anomaly scan: marginal or real problem, a population-based cohort studyAnne Debost-Legrand, Hélène Laurichesse-Delmas, Christine Francannet, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 17, 2004
Interaction between the ADH1C polymorphism and maternal alcohol intake in the risk of nonsyndromic oral clefts: an evaluation of the contribution of child and maternal genotypesCécile Chevrier, Claire Perret, Michel Bahuau, et al.
Birth Defects Research|July 20, 2017
Congenital unilateral renal agenesis: Prevalence, prenatal diagnosis, associated anomalies. Data from two birth-defect registriesHélène Laurichesse Delmas, Monique Kohler, Bérénice Doray, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 3, 2015
Prenatal diagnosis of the VACTERL association using routine ultrasound examinationAnne Debost-Legrand, Carole Goumy, Hélène Laurichesse-Delmas, et al.
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