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C Griscelli

Showing results (281-290 of 358) with videos related to

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Journal of Medical Genetics|July 31, 2001
B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?P Edery, F Le Deist, M L Briard, et al.
Lancet (London, England)|September 3, 1988
Detection of HIV1 DNA in infants and children by means of the polymerase chain reactionF Laure, V Courgnaud, C Rouzioux, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1993
[Cutaneous manifestations disclosing T-cell gamma/delta lymphoma in a 13-year-old-girl]J C Amoric, C Bodemer, J Donadieu, et al.
European Journal of Clinical Investigation|June 1, 1992
Identification of the defective NADPH-oxidase component in chronic granulomatous disease: a study of 57 European familiesC Casimir, M Chetty, M C Bohler, et al.
Lancet (London, England)|November 8, 1986
Bone-marrow transplantation for immunodeficiencies and osteopetrosis: European survey, 1968-1985A Fischer, C Griscelli, W Friedrich, et al.
The New England Journal of Medicine|March 24, 1983
Cellular immune deficiency in two siblings with hereditary orotic aciduriaR Girot, M Hamet, J L Perignon, et al.
Archives Francaises De Pediatrie|January 1, 1985
[Severe combined immune deficiency with hypereosinophilia. Immunologic study of 5 cases]F Le Deist, A Fischer, A Durandy, et al.
American Journal of Medical Genetics|July 15, 1992
Carrier detection and prenatal diagnosis of X-linked agammaglobulinemiaO Journet, A Durandy, M Doussau, et al.
The American Journal of Pathology|June 1, 1983
Evidence that abnormal platelet functions in human Chédiak-Higashi syndrome are the result of a lack of dense bodiesF Rendu, J Breton-Gorius, M Lebret, et al.
Cell|June 17, 1988
Congenital immunodeficiency with a regulatory defect in MHC class II gene expression lacks a specific HLA-DR promoter binding protein, RF-XW Reith, S Satola, C H Sanchez, et al.
Pageof 36

Showing results (281-290 of 358) with videos related to

Sort By:
Pageof 36
Journal of Medical Genetics|July 31, 2001
B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?P Edery, F Le Deist, M L Briard, et al.
Lancet (London, England)|September 3, 1988
Detection of HIV1 DNA in infants and children by means of the polymerase chain reactionF Laure, V Courgnaud, C Rouzioux, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1993
[Cutaneous manifestations disclosing T-cell gamma/delta lymphoma in a 13-year-old-girl]J C Amoric, C Bodemer, J Donadieu, et al.
European Journal of Clinical Investigation|June 1, 1992
Identification of the defective NADPH-oxidase component in chronic granulomatous disease: a study of 57 European familiesC Casimir, M Chetty, M C Bohler, et al.
Lancet (London, England)|November 8, 1986
Bone-marrow transplantation for immunodeficiencies and osteopetrosis: European survey, 1968-1985A Fischer, C Griscelli, W Friedrich, et al.
The New England Journal of Medicine|March 24, 1983
Cellular immune deficiency in two siblings with hereditary orotic aciduriaR Girot, M Hamet, J L Perignon, et al.
Archives Francaises De Pediatrie|January 1, 1985
[Severe combined immune deficiency with hypereosinophilia. Immunologic study of 5 cases]F Le Deist, A Fischer, A Durandy, et al.
American Journal of Medical Genetics|July 15, 1992
Carrier detection and prenatal diagnosis of X-linked agammaglobulinemiaO Journet, A Durandy, M Doussau, et al.
The American Journal of Pathology|June 1, 1983
Evidence that abnormal platelet functions in human Chédiak-Higashi syndrome are the result of a lack of dense bodiesF Rendu, J Breton-Gorius, M Lebret, et al.
Cell|June 17, 1988
Congenital immunodeficiency with a regulatory defect in MHC class II gene expression lacks a specific HLA-DR promoter binding protein, RF-XW Reith, S Satola, C H Sanchez, et al.
Pageof 36