about
The molecular pathology of primary immunodeficienciesToo much, too soon?: Commercial provision of noninvasive prenatal screening for subchromosomal abnormalities and beyondFrequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.Evaluation of 22q11.2 deletion in Cleft Palate patients.DiGeorge syndrome presenting as late onset hypocalcaemia in adulthood.Prenatal diagnosis by array-comparative genomic hybridization.Elevated birth prevalence of conotruncal heart defects in a population with high consanguinity rate.Variety of prenatally diagnosed congenital heart disease in 22q11.2 deletion syndrome.Characteristics of 22q 11.2 deletion syndrome undiagnosed until adulthood: an example suggesting the importance of psychiatric manifestations.Hypocalcaemia in a patient with congenital heart disease.
P2860
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P2860
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Prenatal diagnosis of the 22q11.2 deletion syndrome.
@ast
Prenatal diagnosis of the 22q11.2 deletion syndrome.
@en
Prenatal diagnosis of the 22q11.2 deletion syndrome.
@nl
type
label
Prenatal diagnosis of the 22q11.2 deletion syndrome.
@ast
Prenatal diagnosis of the 22q11.2 deletion syndrome.
@en
Prenatal diagnosis of the 22q11.2 deletion syndrome.
@nl
prefLabel
Prenatal diagnosis of the 22q11.2 deletion syndrome.
@ast
Prenatal diagnosis of the 22q11.2 deletion syndrome.
@en
Prenatal diagnosis of the 22q11.2 deletion syndrome.
@nl
P2860
P1433
P1476
Prenatal diagnosis of the 22q11.2 deletion syndrome.
@en
P2093
Driscoll DA
P2860
P356
10.1097/00125817-200101000-00004
P407
P577
2001-01-01T00:00:00Z
P5875
P6179
1007788231