Showing results (121-130 of 161) with videos related to
Sort By:
Pageof 17
Annales De Genetique|January 1, 1983
Osteoarticular abnormalities and orthopedic complications in children with chromosomal aberrationsG Finidori, P Rigault, J de Grouchy, et al.Annales De Genetique|March 1, 1978
[Assignment of alpha-Fuc to1p in man and the chimpanzee and to chromosome 4 in the African green monkey]N Van Cong, D Weil, C Finaz, et al.Annales De Genetique|September 1, 1976
[Translocation 46,X, t(Y;7)(q122;q11) in a case of male sterility]C Turleau, M F Croquette, J C Fourlinnie, et al.Human Genetics|October 1, 1979
[Localization of the gene for phosphoglycolate phosphatase (PGP) on the chromosome 16 by interspecific hybridization (author's transl)]D Weil, N Van Cong, C Finaz, et al.Human Genetics|January 1, 1984
The gene for human fibroblast interferon (IFB) maps to 9p21L Henry, J Sizun, C Turleau, et al.Clinical Genetics|August 18, 1999
Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletionO Baud, V Cormier-Daire, S Lyonnet, 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.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.Human Genetics|December 31, 2016
Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13Catherine Turleau, J de Grouchy, J L Dufier, et al.Pageof 17