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Showing results (41-50 of 60) with videos related to

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Journal of Medical Genetics|December 1, 1995
No evidence of genetic heterogeneity in dominant optic atrophyD Bonneau, E Souied, S Gerber, et al.
Annales De Biologie Clinique|December 16, 2003
[Call for researchers associated with a biological study of neural tube defects: prospective study of the role of homocysteine in neural tube defects in France]M Candito, C Boisson, P Gaucherand, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1994
[Reflections on 10 years of medically induced abortions in Ille-et-Vilaine]S Schneider, M Roussey, S Odent, et al.
Human Genetics|November 1, 1995
Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analysesC Férec, C Verlingue, P Parent, et al.
European Journal of Pediatrics|August 1, 1996
Abnormal cholesterol biosynthesis in the Smith-Lemli-Opitz and the lethal acrodysgenital syndromesV Cormier-Daire, C Wolf, A Munnich, 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.
Annales De Pediatrie|January 1, 1990
[An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia]S Szpiro-Tapia, J Kaplan, A Pelet, 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.
The Journal of Clinical Endocrinology and Metabolism|April 30, 2010
Progressive osseous heteroplasia: a model for the imprinting effects of GNAS inactivating mutations in humansM Lebrun, N Richard, G Abeguilé, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 21, 2005
[Neonatal screening of cystic fibrosis: diagnostic and ethical problems with mild mutations]M Roussey, A Le Bihannic, M P Audrezet, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|December 1, 1995
No evidence of genetic heterogeneity in dominant optic atrophyD Bonneau, E Souied, S Gerber, et al.
Annales De Biologie Clinique|December 16, 2003
[Call for researchers associated with a biological study of neural tube defects: prospective study of the role of homocysteine in neural tube defects in France]M Candito, C Boisson, P Gaucherand, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1994
[Reflections on 10 years of medically induced abortions in Ille-et-Vilaine]S Schneider, M Roussey, S Odent, et al.
Human Genetics|November 1, 1995
Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analysesC Férec, C Verlingue, P Parent, et al.
European Journal of Pediatrics|August 1, 1996
Abnormal cholesterol biosynthesis in the Smith-Lemli-Opitz and the lethal acrodysgenital syndromesV Cormier-Daire, C Wolf, A Munnich, 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.
Annales De Pediatrie|January 1, 1990
[An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia]S Szpiro-Tapia, J Kaplan, A Pelet, 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.
The Journal of Clinical Endocrinology and Metabolism|April 30, 2010
Progressive osseous heteroplasia: a model for the imprinting effects of GNAS inactivating mutations in humansM Lebrun, N Richard, G Abeguilé, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 21, 2005
[Neonatal screening of cystic fibrosis: diagnostic and ethical problems with mild mutations]M Roussey, A Le Bihannic, M P Audrezet, et al.
Pageof 6