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A Girardet

Showing results (21-30 of 31) with videos related to

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Annales De Genetique|January 1, 1995
[Direct analysis of the frequency of disomy in human sperm using the PRINS technique]I Quenesson, A Girardet, L Coignet, et al.
Cytogenetics and Cell Genetics|January 1, 1996
FISH and PRINS, a strategy for rapid chromosome screening: application to the assessment of aneuploidy in human spermF Pellestor, I Quenesson, L Coignet, et al.
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.
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.
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 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Annales De Genetique|January 1, 1995
[Direct analysis of the frequency of disomy in human sperm using the PRINS technique]I Quenesson, A Girardet, L Coignet, et al.
Cytogenetics and Cell Genetics|January 1, 1996
FISH and PRINS, a strategy for rapid chromosome screening: application to the assessment of aneuploidy in human spermF Pellestor, I Quenesson, L Coignet, et al.
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.
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.
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 4