ロード中...
A 15q13.3 microdeletion segregating with autism
Autism and mental retardation (MR) show high rates of comorbidity and potentially share genetic risk factors. In this study, a rare ∼2 Mb microdeletion involving chromosome band 15q13.3 was detected in a multiplex autism family. This genomic loss lies between distal break points of the Prader–Willi/...
保存先:
| 主要な著者: | , , , , , , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group
2009
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2986268/ https://ncbi.nlm.nih.gov/pubmed/19050728 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2008.228 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|