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American Journal of Medical Genetics|December 1, 1994
Molecular analysis of 53 fragile X families with the probe StB12.3H Puissant, M C Malinge, A Larget-Piet, et al.Prenatal Diagnosis|July 12, 2011
Diagnosis of fetal urinary tract malformations: prenatal management and postnatal outcomeA Ryckewaert-D'Halluin, G Le Bouar, S Odent, et al.Nature Genetics|November 1, 1993
A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1J Kaplan, S Gerber, D Larget-Piet, et al.The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|November 16, 2011
Binder phenotype in mothers affected with autoimmune disordersE Colin, R Touraine, J M Levaillant, et al.American Journal of Human Genetics|May 23, 1998
Mapping of a congenital microcoria locus to 13q31-q32C Rouillac, O Roche, D Marchant, et al.Pathologie-Biologie|February 2, 2010
[Genetic testing in the context of the revision of the French law on bioethics]D Bonneau, S Marlin, D Sanlaville, et al.Human Mutation|April 11, 2001
Mutation analysis of the tyrosinase gene in oculocutaneous albinismO Camand, D Marchant, S Boutboul, et al.Clinical Genetics|January 11, 2016
Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencingC Mouden, C Dubourg, W Carré, et al.Human Molecular Genetics|August 11, 1999
Expression of the Sonic hedgehog (SHH ) gene during early human development and phenotypic expression of new mutations causing holoprosencephalyS Odent, T Atti-Bitach, M Blayau, et al.Clinical Genetics|July 4, 2006
Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndromeC Badens, C Lacoste, N Philip, et al.Pageof 11