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February 19, 1987New England Journal of Medicine

Carrier Detection in X-Linked Agammaglobulinemia by Analysis of X-Chromosome Inactivation

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Authors

EFEric R. FearonUniversité Claude Bernard Lyon 1JWJerry A. WinkelsteinJohns Hopkins UniversityCCCurt I. CivinUniversity of Maryland, Baltimore

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Fearon et al. (1987) studied this question.

synapsesocial.com/papers/6a7d835dc108c8d3ff044a6dhttps://doi.org/10.1056/nejm198702193160802
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5' end of the gene for phosphoglycerate kinase.1986 · 162 citations
  2. 2A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.1983 · 122 citations
  3. 3Expression of the Gene Defect in X-Linked Agammaglobulinemia1986 · 174 citations
  4. 4Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation.1984 · 310 citations
  5. 5MAMMALIAN X-CHROMOSOME INACTIVATION1983 · 644 citations