X chromosome inactivation patterns in haematopoietic cells of female carriers of X-linked severe combined immunodeficiency determined by methylation analysis at the hypervariable DXS255 locus
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03221.x/fullpdf
Reference23 articles.
1. A severe combined immunodeficiency mutation in the mouse;Bosma;Nature,1983
2. Methylation patterns at the hypervariable X chromosome locus DXS255 (M27B): correlation with X inactivation status;Boyd;Genomics,1990
3. Non-random X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immune deficiency;Conley;Proc Natl Acad Sci USA,1988
4. X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings;Conley;J Clin Invest,1990
5. Primordial cell pool size and lineage relationships of five human cell types;Fialkow;Ann Hum Genet,1973
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1. Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologies;Clinical Genetics;2008-06-28
2. Neither uniparental disomy nor skewed X-inactivation explains Rett syndrome;Clinical Genetics;2008-04-23
3. Defining the Cause of Skewed X-Chromosome Inactivation in X-Linked Mental Retardation by Use of a Mouse Model;The American Journal of Human Genetics;2007-06
4. Breakthroughs in the Understanding and Therapy of Primary Immunodeficiency;Pediatric Clinics of North America;1994-08
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