Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2001.600306.x/fullpdf
Reference22 articles.
1. Partial trisomy 14q due to familial t(14q−,11q+) translocation;Fryns;Hum Genet,1977
2. Balanced and unbalanced pericentric inversion of a chromosome 14;Pfeiffer;Hum Genet,1978
3. Duplication of the distal segment of 14q;Atkin;Am J Med Genet,1983
4. Partial trisomy 14 (q23 leads to qter) via segregation of a 14/X translocation;Cohen;Am J Hum Genet,1983
5. Familial pericentric inversion (14) (p11;q24) with a rec dup(q) in one offspring;Kaiser;Clin Genet,1984
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1. A Recurrent De Novo Terminal Duplication of 14q32 in Korean Siblings Associated with Developmental Delay and Intellectual Disability, Growth Retardation, Facial Dysmorphism, and Cerebral Infarction: A Case Report and Literature Review;Genes;2021-09-07
2. Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-Inactivation;Cytogenetic and Genome Research;2020
3. Spread of X-chromosome inactivation into chromosome 15 is associated with Prader–Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation;Human Genetics;2011-07-07
4. Molecular and cytogenetic analysis of the spreading of X inactivation in a girl with microcephaly, mild dysmorphic features and t(X;5)(q22.1;q31.1);European Journal of Human Genetics;2008-02-27
5. Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation;Fertility and Sterility;2006-11
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