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C Turleau

Showing results (91-100 of 155) with videos related to

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Annales De Genetique|March 1, 1976
[Partial 7 q trisomy. One or 2 syndromes? Apropos of a new case]C Turleau, A Rossier, G de Montis, et al.
Human Molecular Genetics|June 1, 1993
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndromeM Jeanpierre, C Turleau, A Aurias, et al.
Annales De Genetique|December 1, 1978
[Satellited Y chromosome (Yqs) and nucleolar organizer occurring de novo]C Turleau, F Chavin-Colin, J Seger, et al.
Human Genetics|January 1, 1984
Conservation of the human COL1A1-TK-GAA synteny and homoeologous assignment in the African green monkey and the baboon (Cercopithecoidae)N Créau-Goldberg, C Turleau, C Cochet, et al.
Annales De Genetique|January 1, 1988
[Interstitial deletion in the long arm of chromosome 7]P Sarda, C Turleau, M O Cabanis, et al.
American Journal of Medical Genetics|August 17, 1999
Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndromeS Briault, S Odent, J Lucas, et al.
Human Molecular Genetics|March 1, 1995
Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastomaV Blanquet, C Turleau, M S Gross-Morand, et al.
Annales De Genetique|January 1, 1989
Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocationsA Sefiani, S Heuertz, C Turleau, et al.
Annales De Genetique|January 1, 1989
The decrease of catalase or esterase D activity in patients with microdeletions of 11p or 13q does not increase their radiosensitivityL Sabatier, F Hoffschir, W A al Achkar, et al.
Annales De Genetique|December 1, 1976
Mapping of the gene for glutathione reductase on chromosome 8A de la Chapelle, A Icen, P Aula, et al.
Pageof 16

Showing results (91-100 of 155) with videos related to

Sort By:
Pageof 16
Annales De Genetique|March 1, 1976
[Partial 7 q trisomy. One or 2 syndromes? Apropos of a new case]C Turleau, A Rossier, G de Montis, et al.
Human Molecular Genetics|June 1, 1993
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndromeM Jeanpierre, C Turleau, A Aurias, et al.
Annales De Genetique|December 1, 1978
[Satellited Y chromosome (Yqs) and nucleolar organizer occurring de novo]C Turleau, F Chavin-Colin, J Seger, et al.
Human Genetics|January 1, 1984
Conservation of the human COL1A1-TK-GAA synteny and homoeologous assignment in the African green monkey and the baboon (Cercopithecoidae)N Créau-Goldberg, C Turleau, C Cochet, et al.
Annales De Genetique|January 1, 1988
[Interstitial deletion in the long arm of chromosome 7]P Sarda, C Turleau, M O Cabanis, et al.
American Journal of Medical Genetics|August 17, 1999
Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndromeS Briault, S Odent, J Lucas, et al.
Human Molecular Genetics|March 1, 1995
Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastomaV Blanquet, C Turleau, M S Gross-Morand, et al.
Annales De Genetique|January 1, 1989
Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocationsA Sefiani, S Heuertz, C Turleau, et al.
Annales De Genetique|January 1, 1989
The decrease of catalase or esterase D activity in patients with microdeletions of 11p or 13q does not increase their radiosensitivityL Sabatier, F Hoffschir, W A al Achkar, et al.
Annales De Genetique|December 1, 1976
Mapping of the gene for glutathione reductase on chromosome 8A de la Chapelle, A Icen, P Aula, et al.
Pageof 16