Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15‐16.1

BACKGROUND: During whole genome microarray‐based comparative genomic hybridisation (array CGH) screening of subjects with idiopathic intellectual disability, we identified two unrelated individuals with a similar de novo interstitial microdeletion at 2p15‐2p16.1. Both individuals share a similar cli...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Rajcan‐Separovic, E, Harvard, C, Liu, X, McGillivray, B, Hall, J G, Qiao, Y, Hurlburt, J, Hildebrand, J, Mickelson, E C R, Holden, J J A, Lewis, M E S
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Group 2007
Konular:
Letter to JMG
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2598046/
https://ncbi.nlm.nih.gov/pubmed/16963482
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.045013
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller