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Annales De Genetique|August 26, 1998
Orofacial cleft defects: inference from nature and nurtureC Houdayer, M BahuauClinical Genetics|December 18, 2002
FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palateM Bahuau, C Houdayer, M Tredano, et al.Clinical Chemistry and Laboratory Medicine|May 9, 2001
Clinical biological and genetic heterogeneity of the inborn errors of pulmonary surfactant metabolismM Tredano, J De Blic, M Griese, et al.Annales De Biologie Clinique|April 3, 2001
[Clinical, biological and genetic heterogeneity of the inborn errors of pulmonary surfactant metabolism: SP-B deficiency and alveolar proteinosis]M Tredano, J D Blic, M Griese, et al.Clinical Chemistry|July 1, 1999
TaqMan PCR-based gene dosage assay for predictive testing in individuals from a cancer family with INK4 locus haploinsufficiencyI Laurendeau, M Bahuau, N Vodovar, et al.Occupational and Environmental Medicine|April 29, 2006
Occupational exposure to organic solvent mixtures during pregnancy and the risk of non-syndromic oral cleftsC Chevrier, B Dananché, M Bahuau, et al.Revue D'Epidemiologie Et De Sante Publique|December 16, 2005
[Periconceptional folates and the prevention of orofacial clefts: role of dietary intakes in France]F Rouget, C Monfort, M Bahuau, et al.Thorax|December 25, 2004
Anti-GM-CSF antibodies in paediatric pulmonary alveolar proteinosisP Latzin, M Tredano, Y Wüst, et al.American Journal of Medical Genetics|August 3, 2001
Pierre Robin sequence and interstitial deletion 2q32.3-q33.2C Houdayer, M F Portnoï, F Vialard, et al.American Journal of Medical Genetics|July 1, 1993
No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome familiesW F Flintoff, M Bahuau, S Lyonnet, et al.Pageof 3