Evaluation of potential modifiers of the palatal phenotype in the 22q11.2 deletion syndrome.
about
Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndromeCharacteristic face: a key indicator for direct diagnosis of 22q11.2 deletions in Chinese velocardiofacial syndrome patients.Clinical and molecular cytogenetic studies of an unrecognised 22q11.2 deletion in three familiesBiallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling.Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion sizeElevated homocysteine and N-methyl-d-aspartate-receptor antibodies as a cause of behavioural and cognitive decline in 22q11.2 deletion syndrome.
P2860
Evaluation of potential modifiers of the palatal phenotype in the 22q11.2 deletion syndrome.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome.
@ast
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome.
@en
type
label
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome.
@ast
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome.
@en
prefLabel
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome.
@ast
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome.
@en
P2093
P2860
P356
P1476
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome.
@en
P2093
Beverly S Emanuel
Cynthia Solot
Deborah A Driscoll
Don LaRossa
Jeanne Manson
Laura E Mitchell
Peter Randall
Richard E Kirschner
Torrey Boland
P2860
P304
P356
10.1597/05-070.1
P407
P577
2006-07-01T00:00:00Z