DiGeorge syndrome: the use of model organisms to dissect complex genetics.
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22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and ReviewWDR55 is a nucleolar modulator of ribosomal RNA synthesis, cell cycle progression, and teleost organ developmentBeta-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1.Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects.Miller-Dieker syndrome: analysis of a human contiguous gene syndrome in the mouse.Identification and characterisation of constitutional chromosome abnormalities using arrays of bacterial artificial chromosomes.Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephalyMyocardin marks the earliest cardiac gene expression and plays an important role in heart development.Roles of retinoic acid signaling in normal and abnormal development of the palate and tongue.Ethylnitrosourea-induced thymus-defective mutants identify roles of KIAA1440, TRRAP, and SKIV2L2 in teleost organ development.Mining OMIM for insight into complex diseases.The role of histone modification and a regulatory single-nucleotide polymorphism (rs2071166) in the Cx43 promoter in patients with TOF.22q11 Deletion Syndrome and Urogenital Manifestations: A Clinicopathological Case Report.Deletion of PTEN and BMPR1A on chromosome 10q23 is not always associated with juvenile polyposis of infancy.Jelly belly protein activates the receptor tyrosine kinase Alk to specify visceral muscle pioneers.Wnt signaling balances specification of the cardiac and pharyngeal muscle fields.Gene expression profiling in the developing secondary palate in the absence of Tbx1 function.Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease
P2860
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P2860
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
description
2002 nî lūn-bûn
@nan
2002 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
@ast
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
@en
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
@nl
type
label
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
@ast
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
@en
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
@nl
prefLabel
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
@ast
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
@en
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
@nl
P356
P1476
DiGeorge syndrome: the use of model organisms to dissect complex genetics.
@en
P2093
Antonio Baldini
P304
P356
10.1093/HMG/11.20.2363
P577
2002-10-01T00:00:00Z