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Sonic hedgehog in temporal control of somite formationGermline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humansOesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiologyThe genetic landscape and clinical implications of vertebral anomalies in VACTERL associationMicroRNAs in the pathogenesis of cystic kidney diseaseNeurobehavioral Alterations in a Genetic Murine Model of Feingold Syndrome 2Advances in Skeletal Dysplasia GeneticsRenal dysplasia characterized by prominent cartilaginous metaplasia lesions in VACTERL association: A case report.MicroRNA-17~92 is required for nephrogenesis and renal functionPhenotypic characterization of miR-92a-/- mice reveals an important function of miR-92a in skeletal development.MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.A fourth case of Feingold syndrome type 2: psychiatric presentation and management.Myocardial Mycn is essential for mouse ventricular wall morphogenesis.Is Duane retraction syndrome part of the VACTERL association?Control of vertebrate development by MYCGenetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literatureHuman diseases caused by germline and somatic abnormalities in microRNA and microRNA-related genes.The Genetics Journey: A Case Report of a Genetic Diagnosis Made 30 Years Later.End-stage renal failure, reflux nephropathy and Feingold's syndrome.[Association esophageal atresia type 3 - microcephaly: an incomplete Feingold syndrome?].Interdigital tissue remodelling in the embryonic limb involves dynamic regulation of the miRNA profiles.A role for miR-19 in the migration of adult-born neurons and schizophrenia.Distinct molecular pathways mediate Mycn and Myc-regulated miR-17-92 microRNA action in Feingold syndrome mouse models.Expanding the phenotype of feingold syndrome-2.Anal atresia, coloboma, microphthalmia, and nasal skin tag in a female patient with 3.5 Mb deletion of 3q26 encompassingSOX2
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Feingold syndrome: clinical review and genetic mapping
@ast
Feingold syndrome: clinical review and genetic mapping
@en
Feingold syndrome: clinical review and genetic mapping
@nl
type
label
Feingold syndrome: clinical review and genetic mapping
@ast
Feingold syndrome: clinical review and genetic mapping
@en
Feingold syndrome: clinical review and genetic mapping
@nl
prefLabel
Feingold syndrome: clinical review and genetic mapping
@ast
Feingold syndrome: clinical review and genetic mapping
@en
Feingold syndrome: clinical review and genetic mapping
@nl
P3181
P356
P1476
Feingold syndrome: clinical review and genetic mapping
@en
P2093
Han G Brunner
Jacopo Celli
P304
P3181
P356
10.1002/AJMG.A.20471
P407
P577
2003-11-01T00:00:00Z