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The Journal of Cell Biology|March 27, 2001
Rab27a: A key to melanosome transport in human melanocytesP Bahadoran, E Aberdam, F Mantoux, et al.Nature Genetics|July 1, 1997
Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va geneE Pastural, F J Barrat, R Dufourcq-Lagelouse, et al.Human Genetics|December 1, 1989
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemiaS Guioli, B Arveiler, B Bardoni, et al.Annual Review of Immunology|January 1, 1997
Naturally occurring primary deficiencies of the immune systemA Fischer, M Cavazzana-Calvo, G De Saint Basile, et al.Human Genetics|October 1, 1987
Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)S Malcolm, G de Saint Basile, B Arveiler, et al.Proceedings of the National Academy of Sciences of the United States of America|January 5, 2000
Diversity, functionality, and stability of the T cell repertoire derived in vivo from a single human T cell precursorP Bousso, V Wahn, I Douagi, et al.Nature Genetics|June 3, 2000
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndromeG Ménasché, E Pastural, J Feldmann, et al.Clinical Immunology and Immunopathology|November 1, 1991
Primary membrane T cell immunodeficienciesF Le Deist, G de Saint Basile, F Mazerolles, et al.American Journal of Human Genetics|September 1, 1996
Genetic and physical mapping of the Chediak-Higashi syndrome on chromosome 1q42-43F J Barrat, L Auloge, E Pastural, et al.American Journal of Human Genetics|January 23, 1999
Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneityR Dufourcq-Lagelouse, N Jabado, F Le Deist, et al.Pageof 9