X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings.

Over 80% of infants with severe combined immunodeficiency (SCID) of unknown genetic etiology are males, yet less than a third of these affected males have a family history of X-linked disease. To help identify new mutations of the X-linked SCID gene and to provide genetic counseling, X chromosome in...

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Main Authors: Conley, M E, Buckley, R H, Hong, R, Guerra-Hanson, C, Roifman, C M, Brochstein, J A, Pahwa, S, Puck, J M
格式: Artigo
語言:Inglês
出版: 1990
主題:
Research Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC296604/
https://ncbi.nlm.nih.gov/pubmed/2332505
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