BAC array CGH reveals genomic aberrations in idiopathic mental retardation-Reference-Cited by-同舟云学术

BAC array CGH reveals genomic aberrations in idiopathic mental retardation

Published:2006-02-01 Issue:3 Volume:140A Page:205-211
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Miyake Noriko,Shimokawa Osamu,Harada Naoki,Sosonkina Nadia,Okubo Aiko,Kawara Hiroki,Okamoto Nobuhiko,Kurosawa Kenji,Kawame Hiroshi,Iwakoshi Mie,Kosho Tomoki,Fukushima Yoshimitsu,Makita Yoshio,Yokoyama Yuji,Yamagata Takanori,Kato Mitsuhiro,Hiraki Yoko,Nomura Masayo,Yoshiura Ko-ichiro,Kishino Tatsuya,Ohta Tohru,Mizuguchi Takeshi,Niikawa Norio,Matsumoto Naomichi

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. True hermaphroditism with partial duplication of chromosome 22 and withoutSRY

2. Copy-number polymorphisms: mining the tip of an iceberg

3. Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype

4. Clinical studies on submicroscopic subtelomeric rearrangements: a checklist

5. Telomeres: a diagnosis at the end of the chromosomes

Cited by 56 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. Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome?;European Journal of Medical Genetics;2019-01

2. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants;Italian Journal of Pediatrics;2016-04-12

3. A de-novo interstitial microduplication involving 2p16.1-p15 and mirroring 2p16.1-p15 microdeletion syndrome: Clinical and molecular analysis;European Journal of Paediatric Neurology;2015-11

4. Control of Type I Error Rates for Oncology Biomarker Discovery with High-Throughput Platforms;Statistical Diagnostics for Cancer;2013-04-08

5. A case of cerebral hypomyelination with spondylo-epi-metaphyseal dysplasia;American Journal of Medical Genetics Part A;2012-12-13