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B le Marec

Showing results (91-100 of 103) with videos related to

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Pediatrie|January 1, 1989
[Neonatal mortality at the Ille-et-Vilaine department. Results in 1987]C Lefrançois, M Hadi, F Letord, et al.
Human Genetics|December 1, 1988
Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosomeS Szpiro-Tapia, A Sefiani, M Guilloud-Bataille, et al.
Pediatrie|January 1, 1993
[Congenital intrahepatic arterio-portal fistula: diagnostic and therapeutic aspects]C Meunier, A Dabadie, P Darnault, 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.
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.
Genomics|October 1, 1992
The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52S Lyonnet, A Pelet, G Royer, et al.
American Journal of Human Genetics|July 1, 1992
Time and space clusters of the French-Canadian M1V phenylketonuria mutation in FranceS Lyonnet, D Melle, M de Braekeleer, 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.
Human Molecular Genetics|June 1, 1993
Fine mapping of the human SCIDX1 locus at Xq12-13.1S Markiewicz, J P DiSanto, J Chelly, et al.
Pageof 11

Showing results (91-100 of 103) with videos related to

Sort By:
Pageof 11
Pediatrie|January 1, 1989
[Neonatal mortality at the Ille-et-Vilaine department. Results in 1987]C Lefrançois, M Hadi, F Letord, et al.
Human Genetics|December 1, 1988
Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosomeS Szpiro-Tapia, A Sefiani, M Guilloud-Bataille, et al.
Pediatrie|January 1, 1993
[Congenital intrahepatic arterio-portal fistula: diagnostic and therapeutic aspects]C Meunier, A Dabadie, P Darnault, 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.
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.
Genomics|October 1, 1992
The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52S Lyonnet, A Pelet, G Royer, et al.
American Journal of Human Genetics|July 1, 1992
Time and space clusters of the French-Canadian M1V phenylketonuria mutation in FranceS Lyonnet, D Melle, M de Braekeleer, 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.
Human Molecular Genetics|June 1, 1993
Fine mapping of the human SCIDX1 locus at Xq12-13.1S Markiewicz, J P DiSanto, J Chelly, et al.
Pageof 11