Subtelomeric rearrangements and copy number variations in people with intellectual disabilities-Reference-Cited by-同舟云学术

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Subtelomeric rearrangements and copy number variations in people with intellectual disabilities

Published:2010-08-30 Issue:10 Volume:54 Page:938-942
ISSN:0964-2633
Container-title:Journal of Intellectual Disability Research
language:en
Short-container-title:

Author:

Christofolini D. M.,De Paula Ramos M. A.,Kulikowski L. D.,Da Silva Bellucco F. T.,Belangero S. I. N.,Brunoni D.,Melaragno M. I.

Publisher

Wiley

Subject

Psychiatry and Mental health,Clinical Neurology,Neurology,Arts and Humanities (miscellaneous),Rehabilitation

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2788.2010.01325.x/fullpdf

Reference36 articles.

1. Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation;Auber;Molecular Cytogenetics,2009

2. Subtelomeric imbalances in phenotypically normal individuals;Balikova;Human Mutation,2007

3. Detection and validation of copy number variation in X-linked mental retardation;Bauters;Cytogenetic and Genome Research,2008

4. Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye;Boehm;Human Mutation,2004

5. Partial trisomy 20p resulting from a recombination of a familial pericentric inversion;Bown;Human Genetics,1986

Cited by 8 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. A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability;Scientific Reports;2018-09-06

2. Post-mortem cytogenomic investigations in patients with congenital malformations;Experimental and Molecular Pathology;2016-08

3. Subtelomeric aberrations in Thai patients with idiopathic mental retardation and autism detected by multiplex ligation-dependent probe amplification;ASIAN BIOMED;2015

4. De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations;Orphanet Journal of Rare Diseases;2015-06-14

5. Comparison of two subtelomeric assays for the screening of chromosomal rearrangements: analysis of 383 patients, literature review and further recommendations;Journal of Applied Genetics;2015-06-12

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