載入...

Comparative deletion mapping at 1p31.3-p32.2 implies NFIA responsible for intellectual disability coupled with macrocephaly and the presence of several other genes for syndromic intellectual disability

BACKGROUND: While chromosome 1 is the largest chromosome in the human genome, less than two dozen cases of interstitial microdeletions in the short arm have been documented. More than half of the 1p microdeletion cases were reported in the pre-microarray era and as a result, the proximal and distal...

全面介紹

Na minha lista:
書目詳細資料
發表在:Mol Cytogenet
Main Authors: Labonne, Jonathan D. J., Shen, Yiping, Kong, Il-Keun, Diamond, Michael P., Layman, Lawrence C., Kim, Hyung-Goo
格式: Artigo
語言:Inglês
出版: BioMed Central 2016
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4797196/
https://ncbi.nlm.nih.gov/pubmed/26997977
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-016-0234-z
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!