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Human Genetics
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July 31, 2019
Genetic architecture of retinoic-acid signaling-associated ocular developmental defects
B Nedelec, J-M Rozet, L Fares Taie
Pediatrie
|
January 1, 1992
[Molecular genetics and prenatal diagnosis]
S Lyonnet, J M Rozet, C Martin, et al.
Human Molecular Genetics
|
June 1, 1994
DsaI polymorphism at the human cone transducin alpha-subunit (GNAT2) detected by PCR
J M Rozet, S Gerber, D Bonneau, et al.
Journal Francais D'Ophtalmologie
|
January 1, 1996
[Rapid demonstration of mutations previously identified in parents at risk of patients with autosomic dominant retinitis pigmentosa]
E Souied, J M Rozet, S Gerber, et al.
Human Molecular Genetics
|
July 1, 1993
Dinucleotide repeat polymorphism at the human recoverin RCVI gene locus on chromosome 17p
H Dollfus, J M Rozet, M A Musarella, et al.
Human Mutation
|
February 6, 1998
Novel intragenic deletions and point mutations of the ornithine transcarbamylase gene in congenital hyperammonemia
P Calvas, B Ségues, J M Rozet, et al.
Journal Francais D'Ophtalmologie
|
March 16, 2005
[Hereditary macular dystrophies]
J-M Rozet, S Gerber, D Ducroq, et al.
Human Molecular Genetics
|
December 1, 1993
Dinucleotide repeat polymorphism at the human protein C inhibitor (PCI) locus
D Larget-Piet, J M Rozet, S Gerber, et al.
Genomics
|
August 1, 1993
Physical and genetic localization of the gamma subunit of the cyclic GMP phosphodiesterase on the long arm of chromosome 17 (17q25)
H Dollfus, M G Mattei, J M Rozet, et al.
Genomics
|
July 15, 1994
Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1
L Oliveira, P Miniou, E Viegas-Pequignot, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 57) with videos related to
Sort By:
Page
of 6
Human Genetics
|
July 31, 2019
Genetic architecture of retinoic-acid signaling-associated ocular developmental defects
B Nedelec, J-M Rozet, L Fares Taie
Pediatrie
|
January 1, 1992
[Molecular genetics and prenatal diagnosis]
S Lyonnet, J M Rozet, C Martin, et al.
Human Molecular Genetics
|
June 1, 1994
DsaI polymorphism at the human cone transducin alpha-subunit (GNAT2) detected by PCR
J M Rozet, S Gerber, D Bonneau, et al.
Journal Francais D'Ophtalmologie
|
January 1, 1996
[Rapid demonstration of mutations previously identified in parents at risk of patients with autosomic dominant retinitis pigmentosa]
E Souied, J M Rozet, S Gerber, et al.
Human Molecular Genetics
|
July 1, 1993
Dinucleotide repeat polymorphism at the human recoverin RCVI gene locus on chromosome 17p
H Dollfus, J M Rozet, M A Musarella, et al.
Human Mutation
|
February 6, 1998
Novel intragenic deletions and point mutations of the ornithine transcarbamylase gene in congenital hyperammonemia
P Calvas, B Ségues, J M Rozet, et al.
Journal Francais D'Ophtalmologie
|
March 16, 2005
[Hereditary macular dystrophies]
J-M Rozet, S Gerber, D Ducroq, et al.
Human Molecular Genetics
|
December 1, 1993
Dinucleotide repeat polymorphism at the human protein C inhibitor (PCI) locus
D Larget-Piet, J M Rozet, S Gerber, et al.
Genomics
|
August 1, 1993
Physical and genetic localization of the gamma subunit of the cyclic GMP phosphodiesterase on the long arm of chromosome 17 (17q25)
H Dollfus, M G Mattei, J M Rozet, et al.
Genomics
|
July 15, 1994
Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1
L Oliveira, P Miniou, E Viegas-Pequignot, et al.
Page
of 6