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S Odent

Showing results (61-70 of 110) with videos related to

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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.
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.
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.
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.
Human Mutation|April 11, 2001
Mutation analysis of the tyrosinase gene in oculocutaneous albinismO Camand, D Marchant, S Boutboul, 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.
Pageof 11

Showing results (61-70 of 110) with videos related to

Sort By:
Pageof 11
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.
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.
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.
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.
Human Mutation|April 11, 2001
Mutation analysis of the tyrosinase gene in oculocutaneous albinismO Camand, D Marchant, S Boutboul, 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.
Pageof 11