Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches-Reference-Cited by-同舟云学术

Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches

Published:2008-01-09 Issue:3 Volume:16 Page:395-400
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Koolen David A,Sistermans Erik A,Nilessen Willy,Knight Samantha J L,Regan Regina,Liu Yan T,Kooy R Frank,Rooms Liesbeth,Romano Corrado,Fichera Marco,Schinzel Albert,Baumer Alessandra,Anderlid Britt-Marie,Schoumans Jacqueline,van Kessel Ad Geurts,Nordenskjold Magnus,de Vries Bert B A

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5201975.pdf

Reference30 articles.

1. de Vries BB, Pfundt R, Leisink M et al: Diagnostic genome profiling in mental retardation. Am J Hum Genet 2005; 77: 606–616.

2. Engels H, Brockschmidt A, Hoischen A et al: DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation. Neurology 2007; 68: 743–750.

3. Krepischi-Santos AC, Vianna-Morgante AM, Jehee FS et al: Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations. Cytogenet Genome Res 2006; 115: 254–261.

4. Menten B, Maas N, Thienpont B et al: Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports. J Med Genet 2006; 43: 625–633.

5. Rosenberg C, Knijnenburg J, Bakker E et al: Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents. J Med Genet 2006; 43: 180–186.

Cited by 13 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. Genomic architecture of human chromosomal diseases;Russian Journal of Genetics;2016-05

2. Whole-genome array as a first-line cytogenetic test in prenatal diagnosis;Ultrasound in Obstetrics & Gynecology;2015-04

3. A de novo POU3F3 Deletion in a Boy with Intellectual Disability and Dysmorphic Features;Molecular Syndromology;2013

4. Educational Attainment: A Genome Wide Association Study in 9538 Australians;PLoS ONE;2011-06-09

5. Fine-Scale Survey of X Chromosome Copy Number Variants and Indels Underlying Intellectual Disability;The American Journal of Human Genetics;2010-08