A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.
about
Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2)A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.RAR-related orphan receptor A isoform 1 (RORa1) is disrupted by a balanced translocation t(4;15)(q22.3;q21.3) associated with severe obesity.
P2860
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.
description
1990 nî lūn-bûn
@nan
1990 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.
@ast
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.
@en
type
label
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.
@ast
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.
@en
prefLabel
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.
@ast
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.
@en
P2093
P2860
P356
P1476
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.
@en
P2093
P2860
P304
P356
10.1136/JMG.27.10.637
P407
P577
1990-10-01T00:00:00Z