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Human Genetics|December 1, 1991
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineagesL D Notarangelo, O Parolini, A Albertini, et al.Neurogenetics|February 7, 2001
Evidence that allelic variants of the spinocerebellar ataxia type 2 gene influence susceptibility to multiple sclerosisJ Chataway, S Sawcer, F Coraddu, et al.Journal of Neuroimmunology|August 3, 1999
A screen of candidates from peaks of linkage: evidence for the involvement of myeloperoxidase in multiple sclerosisJ Chataway, S Sawcer, R Feakes, et al.Nature Genetics|August 1, 1996
A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22S Sawcer, H B Jones, R Feakes, et al.Genetic Epidemiology|May 14, 1999
Exploring the dense mapping of a region of potential linkage in complex disease: an example in multiple sclerosisR Feakes, S Sawcer, J Chataway, et al.Human Genetics|February 1, 1992
The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditismG D Berkovitz, P Y Fechner, S M Marcantonio, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1995
A family of rapidly evolving genes from the sex reversal critical region in Xp21B Dabovic, E Zanaria, B Bardoni, et al.Human Genetics|December 1, 1989
Cytogenetic and molecular analysis of an unbalanced translocation (X;7) (q28;p15) in a dysmorphic girlA Caiulo, B Bardoni, G Camerino, et al.Human Genetics|May 1, 1991
X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric regionM L Mostacciuolo, E Müller, P Fardin, et al.Journal of Molecular Biology|April 20, 1985
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosomeJ Wolfe, S M Darling, R P Erickson, et al.Pageof 21