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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:J Clin Invest
Main Authors: Conley, M E, Buckley, R H, Hong, R, Guerra-Hanson, C, Roifman, C M, Brochstein, J A, Pahwa, S, Puck, J M
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Clinical Investigation 1990
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC296604/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2332505/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI114603
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker