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J-M Rozet

Showing results (1-10 of 57) with videos related to

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Human Genetics|July 31, 2019
Genetic architecture of retinoic-acid signaling-associated ocular developmental defectsB 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 PCRJ 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 17pH 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 hyperammonemiaP 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) locusD 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 17p13.1L Oliveira, P Miniou, E Viegas-Pequignot, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Human Genetics|July 31, 2019
Genetic architecture of retinoic-acid signaling-associated ocular developmental defectsB 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 PCRJ 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 17pH 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 hyperammonemiaP 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) locusD 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 17p13.1L Oliveira, P Miniou, E Viegas-Pequignot, et al.
Pageof 6