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. 1989 May 11;17(9):3619. doi: 10.1093/nar/17.9.3619

Nsi I RFLP at the X-linked chronic granulomatous disease locus (CYBB).

L Battat 1, U Francke 1
PMCID: PMC317829  PMID: 2566976

Abstract

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These references are in PubMed. This may not be the complete list of references from this article.

  1. Francke U. Random X inactivation resulting in mosaic nullisomy of region Xp21.1----p21.3 associated with heterozygosity for ornithine transcarbamylase deficiency and for chronic granulomatous disease. Cytogenet Cell Genet. 1984;38(4):298–307. doi: 10.1159/000132078. [DOI] [PubMed] [Google Scholar]

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