Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes
about
Hearing loss in a mouse model of 22q11.2 Deletion Syndrome.Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndromeCanalization, developmental stability, and morphological integration in primate limbsTbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.Evaluation of potential modifiers of the palatal phenotype in the 22q11.2 deletion syndrome.Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndromeClinical and molecular cytogenetic studies of an unrecognised 22q11.2 deletion in three familiesGenotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients.Diagnosis of Fanconi anemia by diepoxybutane analysis.Cytogenetics and gene discovery in psychiatric disorders.Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literature.Cellular and molecular events during early thymus development.Immunodeficiency and autoimmunity in 22q11.2 deletion syndrome.Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndrome.Immunological aspects of 22q11.2 deletion syndrome.Gene discovery and functional assessment of rare copy-number variants in neurodevelopmental disorders.Biallelic 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 sizeFunctional attenuation of UFD1l, a 22q11.2 deletion syndrome candidate gene, leads to cardiac outflow septation defects in chicken embryos.Chromosome 22q11.2 duplication is rare in a population-based cohort of Danish children with cardiovascular malformations.The impact of hypocalcemia on full scale IQ in patients with 22q11.2 deletion syndrome
P2860
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P2860
Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes
description
2001 nî lūn-bûn
@nan
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին 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
Genetic factors are major dete ...... he DiGeorge/del22q11 syndromes
@ast
Genetic factors are major dete ...... he DiGeorge/del22q11 syndromes
@en
type
label
Genetic factors are major dete ...... he DiGeorge/del22q11 syndromes
@ast
Genetic factors are major dete ...... he DiGeorge/del22q11 syndromes
@en
prefLabel
Genetic factors are major dete ...... he DiGeorge/del22q11 syndromes
@ast
Genetic factors are major dete ...... he DiGeorge/del22q11 syndromes
@en
P2093
P2860
P356
P1476
Genetic factors are major dete ...... he DiGeorge/del22q11 syndromes
@en
P2093
P2860
P304
11428-11431
P356
10.1073/PNAS.201127298
P407
P577
2001-09-18T00:00:00Z