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Pediatrie
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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 chromosome
S 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 review
S Odent, B Le Marec, A Toutain, et al.
Genomics
|
October 1, 1992
The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52
S 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 France
S 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 20
I 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 gastroschisis
P Poulain, J Milon, B Frémont, et al.
Human Molecular Genetics
|
June 1, 1993
Fine mapping of the human SCIDX1 locus at Xq12-13.1
S Markiewicz, J P DiSanto, J Chelly, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 103) with videos related to
Sort By:
Page
of 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 chromosome
S 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 review
S Odent, B Le Marec, A Toutain, et al.
Genomics
|
October 1, 1992
The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52
S 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 France
S 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 20
I 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 gastroschisis
P Poulain, J Milon, B Frémont, et al.
Human Molecular Genetics
|
June 1, 1993
Fine mapping of the human SCIDX1 locus at Xq12-13.1
S Markiewicz, J P DiSanto, J Chelly, et al.
Page
of 11