Unusual X-chromosome inactivation pattern in patients with Xp11.23-p11.22 duplication: Report and review
Author:
Affiliation:
1. Division of Genetics; Department of Morphology and Genetics; Universidade Federal de São Paulo; São Paulo Brazil
2. Department of Biochemistry; Universidade Federal de São Paulo; São Paulo Brazil
Funder
São Paulo Research Foundation
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference14 articles.
1. X chromosome-inactivation patterns of 1,005 phenotypically unaffected females;Amos-Landgraf;Am J Hum Genet,2006
2. Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome;Araujo;Braz J Med Biol Res,2008
3. X-inactivation profile reveals extensive variability in X-linked gene expression in females;Carrel;Nature,2005
4. Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter→q24::q21.32→qter) and random X inactivation;Carrozzo;Am J Med Genet,1997
5. X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes;Disteche;Hum Genet,1984
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