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A GIRARDET

Showing results (31-40 of 41) with videos related to

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American Journal of Human Genetics|January 13, 2000
Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typingA Girardet, M S McPeek, E P Leeflang, et al.
Molecular Human Reproduction|June 13, 2003
Specific detection of deleted and non-deleted dystrophin exons together with gender assignment in preimplantation genetic diagnosis of Duchenne muscular dystrophyA Girardet, S Hamamah, H Déchaud, et al.
Molecular Human Reproduction|February 6, 2003
First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markersA Girardet, S Hamamah, T Anahory, et al.
Clinical Genetics|April 26, 2014
Preimplantation genetic diagnosis for cystic fibrosis: the Montpellier center's 10-year experienceA Girardet, A Ishmukhametova, M Willems, et al.
Clinical Genetics|September 14, 2007
Negative genetic neonatal screening for cystic fibrosis caused by compound heterozygosity for two large CFTR rearrangementsA Girardet, C Guittard, J-P Altieri, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 17, 2020
Genetic counseling for cystic fibrosis: A basic model with new challengesE Bieth, J Nectoux, A Girardet, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Direct estimation of the recombination frequency between the RB1 gene and two closely linked microsatellites using sperm typingA Girardet, S Lien, E P Leeflang, et al.
American Journal of Human Genetics|December 5, 1998
Evidence of somatic and germinal mosaicism in pseudo-low-penetrant hereditary retinoblastoma, by constitutional and single-sperm mutation analysisF L Munier, F Thonney, A Girardet, et al.
Human Genetics|January 28, 1999
Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African familyF Macari, C Lautier, A Girardet, et al.
Pathologie-Biologie|December 4, 2009
[Genetic mutation databases: stakes and perspectives for orphan genetic diseases]V Humbertclaude, S Tuffery-Giraud, C Bareil, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|January 13, 2000
Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typingA Girardet, M S McPeek, E P Leeflang, et al.
Molecular Human Reproduction|June 13, 2003
Specific detection of deleted and non-deleted dystrophin exons together with gender assignment in preimplantation genetic diagnosis of Duchenne muscular dystrophyA Girardet, S Hamamah, H Déchaud, et al.
Molecular Human Reproduction|February 6, 2003
First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markersA Girardet, S Hamamah, T Anahory, et al.
Clinical Genetics|April 26, 2014
Preimplantation genetic diagnosis for cystic fibrosis: the Montpellier center's 10-year experienceA Girardet, A Ishmukhametova, M Willems, et al.
Clinical Genetics|September 14, 2007
Negative genetic neonatal screening for cystic fibrosis caused by compound heterozygosity for two large CFTR rearrangementsA Girardet, C Guittard, J-P Altieri, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 17, 2020
Genetic counseling for cystic fibrosis: A basic model with new challengesE Bieth, J Nectoux, A Girardet, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Direct estimation of the recombination frequency between the RB1 gene and two closely linked microsatellites using sperm typingA Girardet, S Lien, E P Leeflang, et al.
American Journal of Human Genetics|December 5, 1998
Evidence of somatic and germinal mosaicism in pseudo-low-penetrant hereditary retinoblastoma, by constitutional and single-sperm mutation analysisF L Munier, F Thonney, A Girardet, et al.
Human Genetics|January 28, 1999
Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African familyF Macari, C Lautier, A Girardet, et al.
Pathologie-Biologie|December 4, 2009
[Genetic mutation databases: stakes and perspectives for orphan genetic diseases]V Humbertclaude, S Tuffery-Giraud, C Bareil, et al.
Pageof 5