X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00275190.pdf
Reference38 articles.
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3. Cohen M, Ratazzi MC (1971) Cytological and biochemical correlation of late X-chromosome replication and gene inactivation in the male. Proc Natl Acad Sci USA 68:544?548
4. Couturier J, Dutrillaux B, Garber P, Raoul O, Croquette MF, Fourlinnie JC, Maillard E (1979) Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21). Hum Genet 49:319?326
5. de la Chapelle A, Herva R, Koivisto M, Aula P (1981) A deletion in chromosome 22 can cause DiGeorge syndrome. Hum Genet 57:253?256
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4. Unusual X-chromosome inactivation pattern in patients with Xp11.23-p11.22 duplication: Report and review;American Journal of Medical Genetics Part A;2016-09-08
5. Spread of X-chromosome inactivation into autosomal sequences: role for DNA elements, chromatin features and chromosomal domains;Human Molecular Genetics;2013-10-24
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