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F Thonney

Showing results (11-20 of 26) with videos related to

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Ophthalmic Paediatrics and Genetics|June 1, 1989
Constitutional karyotype in retinoblastoma. Case report and review of literatureF Munier, G Pescia, M Jotterand-Bellomo, et al.
Revue Medicale De La Suisse Romande|April 1, 1993
[Towards systematic screening for mucoviscidosis?]G Pescia, G Van Melle, F Thonney, et al.
Revue Medicale De La Suisse Romande|July 27, 2000
[Fluorescent in situ hybridization (FISH). Diagnostic aide in certain chromosomal anomalies]A Zankl, M C Addor, F Thonney, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1996
Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counselingF L Munier, F Thonney, A Balmer, et al.
Revue Medicale De La Suisse Romande|April 1, 1993
[Molecular analysis of 68 Swiss-Romance subjects at risk for fragile X syndrome]D F Schorderet, F Thonney, N Pillet, et al.
Ophthalmic Genetics|March 23, 2001
Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomaliesL Lavanchy, F L Munier, P Cousin, et al.
Pediatric Research|October 1, 1991
Association between haplotypes and specific mutations in Swiss cystic fibrosis familiesS Liechti-Gallati, N Malik, M Alkan, et al.
Annales De Genetique|January 1, 1988
Cytogenetic analysis of 570 first trimester chorionic villi samplings: technique and resultsM Jotterand-Bellomo, G Pescia, H Nguyen The, et al.
Human Genetics|July 1, 1992
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility geneF Munier, M A Spence, G Pescia, et al.
American Journal of Medical Genetics|January 9, 2001
Complex chromosome rearrangement in a girl with an incomplete form of Beckwith-Wiedemann syndromeA Zankl, M C Addor, A C Gaide, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Ophthalmic Paediatrics and Genetics|June 1, 1989
Constitutional karyotype in retinoblastoma. Case report and review of literatureF Munier, G Pescia, M Jotterand-Bellomo, et al.
Revue Medicale De La Suisse Romande|April 1, 1993
[Towards systematic screening for mucoviscidosis?]G Pescia, G Van Melle, F Thonney, et al.
Revue Medicale De La Suisse Romande|July 27, 2000
[Fluorescent in situ hybridization (FISH). Diagnostic aide in certain chromosomal anomalies]A Zankl, M C Addor, F Thonney, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1996
Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counselingF L Munier, F Thonney, A Balmer, et al.
Revue Medicale De La Suisse Romande|April 1, 1993
[Molecular analysis of 68 Swiss-Romance subjects at risk for fragile X syndrome]D F Schorderet, F Thonney, N Pillet, et al.
Ophthalmic Genetics|March 23, 2001
Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomaliesL Lavanchy, F L Munier, P Cousin, et al.
Pediatric Research|October 1, 1991
Association between haplotypes and specific mutations in Swiss cystic fibrosis familiesS Liechti-Gallati, N Malik, M Alkan, et al.
Annales De Genetique|January 1, 1988
Cytogenetic analysis of 570 first trimester chorionic villi samplings: technique and resultsM Jotterand-Bellomo, G Pescia, H Nguyen The, et al.
Human Genetics|July 1, 1992
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility geneF Munier, M A Spence, G Pescia, et al.
American Journal of Medical Genetics|January 9, 2001
Complex chromosome rearrangement in a girl with an incomplete form of Beckwith-Wiedemann syndromeA Zankl, M C Addor, A C Gaide, et al.
Pageof 3