Application of carrier testing to genetic counseling for X-linked agammaglobulinemia.

Bruton X-linked agammaglobulinemia (XLA) is a phenotypically recessive genetic disorder of B lymphocyte development. Female carriers of XLA, although asymptomatic, have a characteristic B cell lineage-specific skewing of the pattern of X inactivation. Skewing apparently results from defective growth...

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Bibliographische Detailangaben
Hauptverfasser: Allen, R. C., Nachtman, R. G., Rosenblatt, H. M., Belmont, J. W.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 1994
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1918059/
https://ncbi.nlm.nih.gov/pubmed/7506482
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