Subtelomeric rearrangements in Polish subjects with intellectual disability and dysmorphic features-Reference-Cited by-同舟云学术

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Subtelomeric rearrangements in Polish subjects with intellectual disability and dysmorphic features

Published:2010-06 Issue:2 Volume:51 Page:215-217
ISSN:1234-1983
Container-title:Journal of Applied Genetics
language:en
Short-container-title:J Appl Genet

Author:

Bogdanowicz J.,Pawłowska B.,Ilnicka A.,Gawlik-Zawiślak S.,Jóźwiak A.,Sobiczewska B.,Zdzienicka E.,Korniszewski L.,Zaremba J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF03195731.pdf

Reference7 articles.

1. Fan YS, Zhang Y, Speevak M, Farrell S, Jung J, Siu V, 2001. Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes. Genetics in Medicine 3: 416–421.

2. Flint J, Wilkie AOM, Buckle VJ, Winter RM, Holland AJ, Mc Dermid HE, 1995. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nat Genet 9: 132–139.

3. Giraudeau F, Aubert D, Young I, Horsley S, Knight S, Kearney L, et al. 1997. Molecular-cytogenetic detection of a deletion of 1p36.3 leads to a revised estimate of the frequency of subtelomeric rearrangements in idiopathic mental retardation. J Med Genet 34: 314–317.

4. [ISCN] An International System for Human Cytogenetic Nomenclature, 2009. Ed.: Shaffer LG, Slovak ML, Campbell LJ, KARGER, Basel: 111.

5. Karnebeek CDM, Jansweijer M, Leenders A, Offringa M, Hennekam R, 2005. Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness. Eur J Hum Genet 13, 6–25.

Cited by 4 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. Screening for Subtelomeric Rearrangements in Thai Patients with Intellectual Disabilities Using FISH and Review of Literature on Subtelomeric FISH in 15,591 Cases with Intellectual Disabilities;Genetics Research International;2016-10-16

2. Mental retardation and autism associated with recurrent 16p11.2 microdeletion: incomplete penetrance and variable expressivity;Journal of Applied Genetics;2011-09-20

3. X inactivation testing for identifying a non-syndromic X-linked mental retardation gene;Journal of Applied Genetics;2011-05-17

4. Screening for subtle chromosomal rearrangements in an Egyptian sample of children with unexplained mental retardation;Egyptian Journal of Medical Human Genetics;2011-05

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