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D Bonneau

Showing results (101-110 of 143) with videos related to

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Journal of Perinatology : Official Journal of the California Perinatal Association|December 31, 2013
Fetal intracerebral hemorrhage and cataract: think COL4A1E Colin, L Sentilhes, A Sarfati, 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.
Journal of Medical Genetics|September 1, 1992
Phenotype-genotype correlations in X linked retinitis pigmentosaJ Kaplan, A Pelet, C Martin, et al.
The Journal of Pathology|November 5, 1999
Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2H R Harach, F Lesueur, P Amati, et al.
Human Molecular Genetics|August 1, 1994
Five novel missense mutations of the rhodopsin gene in autosomal dominant retinitis pigmentosaE Souied, S Gerber, J M Rozet, et al.
American Journal of Human Genetics|February 1, 1995
A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13S Gerber, J M Rozet, D Bonneau, et al.
American Journal of Human Genetics|February 1, 1995
A novel microsatellite DNA marker at locus D7S1870 detects hemizygosity in 75% of patients with Williams syndromeB Gilbert-Dussardier, D Bonneau, N Gigarel, et al.
European Neurology|July 17, 2012
OPA3--related autosomal dominant optic atrophy and cataract with ataxia and areflexiaX Ayrignac, C Liauzun, G Lenaers, et al.
Human Molecular Genetics|August 1, 1995
A gene for Leber's congenital amaurosis maps to chromosome 17pA Camuzat, H Dollfus, J M Rozet, et al.
Genomics|December 1, 1992
A gene for Usher syndrome type I (USH1A) maps to chromosome 14qJ Kaplan, S Gerber, D Bonneau, et al.
Pageof 15

Showing results (101-110 of 143) with videos related to

Sort By:
Pageof 15
Journal of Perinatology : Official Journal of the California Perinatal Association|December 31, 2013
Fetal intracerebral hemorrhage and cataract: think COL4A1E Colin, L Sentilhes, A Sarfati, 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.
Journal of Medical Genetics|September 1, 1992
Phenotype-genotype correlations in X linked retinitis pigmentosaJ Kaplan, A Pelet, C Martin, et al.
The Journal of Pathology|November 5, 1999
Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2H R Harach, F Lesueur, P Amati, et al.
Human Molecular Genetics|August 1, 1994
Five novel missense mutations of the rhodopsin gene in autosomal dominant retinitis pigmentosaE Souied, S Gerber, J M Rozet, et al.
American Journal of Human Genetics|February 1, 1995
A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13S Gerber, J M Rozet, D Bonneau, et al.
American Journal of Human Genetics|February 1, 1995
A novel microsatellite DNA marker at locus D7S1870 detects hemizygosity in 75% of patients with Williams syndromeB Gilbert-Dussardier, D Bonneau, N Gigarel, et al.
European Neurology|July 17, 2012
OPA3--related autosomal dominant optic atrophy and cataract with ataxia and areflexiaX Ayrignac, C Liauzun, G Lenaers, et al.
Human Molecular Genetics|August 1, 1995
A gene for Leber's congenital amaurosis maps to chromosome 17pA Camuzat, H Dollfus, J M Rozet, et al.
Genomics|December 1, 1992
A gene for Usher syndrome type I (USH1A) maps to chromosome 14qJ Kaplan, S Gerber, D Bonneau, et al.
Pageof 15