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C Delozier-Blanchet

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Genetic and cytogenetic aspects]C Delozier-Blanchet, M Vekemans
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 5, 1997
[Chromosome mosaicism and intrauterine growth retardation]C DeLozier-Blanchet, M Vekemans
Annales De Genetique|January 1, 1990
Reflections on small supernumerary (marker) chromosomes: could imprinting and isodisomy play a role in the phenotypic expression of hyperdiploidy?S Dahoun-Hadorn, C Delozier-Blanchet
Pediatric Research|October 1, 1994
Prenatal diagnosis of collagen disorders by direct biochemical analysis of chorionic villus biopsiesM Raghunath, B Steinmann, C Delozier-Blanchet, 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.
Schweizerische Rundschau Fur Medizin Praxis = Revue Suisse De Medecine Praxis|May 8, 1984
[Genotypes and phenotypes in a family with mental retardation and fragility of the X chromosomes]E Engel, L Crippa, C Delozier-Blanchet, et al.
The New England Journal of Medicine|December 12, 1991
Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardationF Rousseau, D Heitz, V Biancalana, et al.
Human Mutation|December 19, 2001
Molecular and clinical characteristics in 32 families affected with familial adenomatous polyposisP Hutter, C Rey-Berthod, P O Chappuis, et al.
Journal of Medical Genetics|August 1, 1996
Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutationP Hutter, A Couturier, R J Scott, et al.
Swiss Surgery = Schweizer Chirurgie = Chirurgie Suisse = Chirurgia Svizzera|June 16, 2001
[Multidisciplinary management of hereditary colorectal cancer]C Soravia, C Delozier-Blanchet, J L Blouin, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Genetic and cytogenetic aspects]C Delozier-Blanchet, M Vekemans
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 5, 1997
[Chromosome mosaicism and intrauterine growth retardation]C DeLozier-Blanchet, M Vekemans
Annales De Genetique|January 1, 1990
Reflections on small supernumerary (marker) chromosomes: could imprinting and isodisomy play a role in the phenotypic expression of hyperdiploidy?S Dahoun-Hadorn, C Delozier-Blanchet
Pediatric Research|October 1, 1994
Prenatal diagnosis of collagen disorders by direct biochemical analysis of chorionic villus biopsiesM Raghunath, B Steinmann, C Delozier-Blanchet, 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.
Schweizerische Rundschau Fur Medizin Praxis = Revue Suisse De Medecine Praxis|May 8, 1984
[Genotypes and phenotypes in a family with mental retardation and fragility of the X chromosomes]E Engel, L Crippa, C Delozier-Blanchet, et al.
The New England Journal of Medicine|December 12, 1991
Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardationF Rousseau, D Heitz, V Biancalana, et al.
Human Mutation|December 19, 2001
Molecular and clinical characteristics in 32 families affected with familial adenomatous polyposisP Hutter, C Rey-Berthod, P O Chappuis, et al.
Journal of Medical Genetics|August 1, 1996
Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutationP Hutter, A Couturier, R J Scott, et al.
Swiss Surgery = Schweizer Chirurgie = Chirurgie Suisse = Chirurgia Svizzera|June 16, 2001
[Multidisciplinary management of hereditary colorectal cancer]C Soravia, C Delozier-Blanchet, J L Blouin, et al.
Pageof 2