about
Chromosome 3q29 deletion with gastrointestinal malformation: a case reportA novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial featuresRecurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delays.The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1.Identification of novel genomic imbalances in Saudi patients with congenital heart disease.
P2860
description
1987 nî lūn-bûn
@nan
1987 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
A case of de novo interstitial deletion 3q
@ast
A case of de novo interstitial deletion 3q
@en
type
label
A case of de novo interstitial deletion 3q
@ast
A case of de novo interstitial deletion 3q
@en
prefLabel
A case of de novo interstitial deletion 3q
@ast
A case of de novo interstitial deletion 3q
@en
P2093
P2860
P1476
A case of de novo interstitial deletion 3q
@en
P2093
P2860
P304
P407
P577
1987-05-01T00:00:00Z