Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association - Wikidata - awgldk - TriplyDB

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

http://www.wikidata.org/entity/Q34916997

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VACTERL/VATER Association The genetic landscape and clinical implications of vertebral anomalies in VACTERL association The OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal death Genomic imbalances in pediatric patients with chronic kidney disease.Considering the Embryopathogenesis of VACTERL Association Anorectal malformations associated with esophageal atresia in neonates.Combination of Miller-Dieker syndrome and VACTERL association causes extremely severe clinical presentation.Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.

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Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

http://www.wikidata.org/entity/Q34916997

description

2011 nî lūn-bûn

@nan

2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2011年の論文

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2011年論文

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2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

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name

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

@ast

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

@en

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

@nl

type

label

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

@ast

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

@en

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

@nl

prefLabel

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

@ast

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

@en

Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

@nl

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J.EJMG.2011.01.007

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European Journal of Medical Genetics

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Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association

@en

P2093

Amelia A Keaton

http://www.w3.org/2001/XMLSchema#string

Aparna Kamat

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Benjamin D Solomon

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Daniel E Pineda-Alvarez

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Manu S Raam

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Nicole Warren-Mora

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Nneamaka B Agochukwu

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Settara C Chandrasekharappa

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P2860

Haploinsufficiency of the forkhead gene Foxf1, a target for sonic hedgehog signaling, causes lung and foregut malformations

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations

Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology

Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformations

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

A population study of the VACTERL association: evidence for its etiologic heterogeneity

FoxF1 and FoxL1 link hedgehog signaling and the control of epithelial proliferation in the developing stomach and intestine

The VACTERL association: lessons from the Sonic hedgehog pathway.

Consideration of VACTERL association in patients with trisomy 21.

A novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation, and features of VATER association.

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323-328

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scholarly article

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10.1016/J.EJMG.2011.01.007

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3

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54

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49830345

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21315191

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