Alteration of rRNA gene copy number and expression in patients with intellectual disability and heteromorphic acrocentric chromosomes-Reference-Cited by-同舟云学术

Alteration of rRNA gene copy number and expression in patients with intellectual disability and heteromorphic acrocentric chromosomes

Published:2018-04 Issue:2 Volume:19 Page:129-134
ISSN:1110-8630
Container-title:Egyptian Journal of Medical Human Genetics
language:en
Short-container-title:Egyptian Journal of Medical Human Genetics

Author:

Kolesnikova Irina S.,Dolskiy Alexander A.,Lemskaya Natalya A.,Maksimova Yulia V.,Shorina Asia R.,Graphodatsky Alexander S.,Galanina Ekaterina M.,Yudkin Dmitry V.

Funder

Russian Science Foundation

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical)

Reference26 articles.

1. Genetic studies in intellectual disability and related disorders;Vissers;Nat Rev Genet,2016

2. Heumann G Familial 13p+ chromosome with mental retardation and dysmorphic features of two children;Stoll;Hum Genet,1976

3. Human inherited marker chromosome 22 short arm enlargement: investigation of rDNA gene multiplicity, Ag banding size and acrocentric association;Bernstein;Hum Genet,1981

4. Amplification of (GACA)n simple repeats in an exceptional 14p+ marker chromosome;Schmid;Hum Genet,1994

5. Prenatal diagnosis of a 13p+ caryotype;Soudek;Hum Genet,1979

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. First discovered, long out of sight, finally visible: ribosomal DNA;Trends in Genetics;2022-06

2. A rare familial rearrangement of chromosomes 9 and 15 associated with intellectual disability: a clinical and molecular study;Molecular Cytogenetics;2021-10-04

3. Copy number variations of satellite III (1q12) and ribosomal repeats in health and schizophrenia;Schizophrenia Research;2020-09

4. B cell humoral response and differentiation is regulated by the non-canonical poly(A) polymerase TENT5C;2019-07-09

5. Robertsonian translocation 13/14 associated with rRNA genes overexpression and intellectual disability;Egyptian Journal of Medical Human Genetics;2018-04