(Q37613190)

English

Genetic 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 literature

scientific article published on 12 October 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

4 references

21 March 2019

22 April 2019

11 December 2019

22 December 2019

Genetic 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 literature (English)

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

esophageal atresia

4 references

21 March 2019

22 April 2019

11 December 2019

22 December 2019

tracheoesophageal fistula

4 references

21 March 2019

22 April 2019

11 December 2019

22 December 2019

DNA-binding protein

1 reference

11 December 2019

transcription factor

1 reference

22 December 2019

VACTERL association

1 reference

based on heuristic

inferred from title

author name string

Charles Shaw-Smith

1

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

12 October 2009

5 references

Europe PubMed Central

PMC publication ID

21 August 2017

21 March 2019

22 April 2019

11 December 2019

22 December 2019

European Journal of Medical Genetics

5 references

Europe PubMed Central

PMC publication ID

21 August 2017

21 March 2019

22 April 2019

11 December 2019

22 December 2019

53

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

6-13

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

copyright license

Creative Commons Attribution 3.0 Unported

4 references

Europe PubMed Central

21 March 2019

Europe PubMed Central

22 April 2019

Europe PubMed Central

11 December 2019

Europe PubMed Central

22 December 2019

copyright status

0 references

on focus list of Wikimedia project

0 references

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

1 reference

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1 reference

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1 reference

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

1 reference

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Cytogenetic Technology — Genotype and Phenotype

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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Chromosomal anomalies in the aetiology of oesophageal atresia and tracheo-oesophageal fistula

1 reference

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Transcriptional control of lung morphogenesis

1 reference

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Morphogenesis of the trachea and esophagus: current players and new roles for noggin and Bmps

1 reference

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23 August 2017

Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome

1 reference

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1 reference

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Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome

1 reference

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23 August 2017

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

1 reference

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23 August 2017

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

1 reference

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23 August 2017

Genetic players in esophageal atresia and tracheoesophageal fistula

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2809919

23 August 2017

Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations

1 reference

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X-linked inheritance of Fanconi anemia complementation group B

1 reference

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Sox2 deficiency causes neurodegeneration and impaired neurogenesis in the adult mouse brain

1 reference

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Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

1 reference

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Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features

1 reference

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Feingold syndrome: clinical review and genetic mapping

1 reference

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Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24

1 reference

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Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin

1 reference

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1 reference

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1 reference

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1 reference

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Distal 13q Deletion Syndrome and the VACTERL association: case report, literature review, and possible implications

1 reference

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1 reference

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1 reference

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Hedgehog signals regulate multiple aspects of gastrointestinal development

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Fryns syndrome: report on 8 new cases

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5.9 Mb microdeletion in chromosome band 17q22-q23.2 associated with tracheo-esophageal fistula and conductive hearing loss.

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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Foxl1-deficient mice exhibit aberrant epithelial cell positioning resulting from dysregulated EphB/EphrinB expression in the small intestine

1 reference

https://pubmed.ncbi.nlm.nih.gov/19822228

12 December 2020

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inferred from PubMed ID database lookup

Phenotype and 244k array-CGH characterization of chromosome 13q deletions: an update of the phenotypic map of 13q21.1-qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/19822228

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

'Microgastria--limb reduction' complex with congenital heart disease and twinning

1 reference

https://pubmed.ncbi.nlm.nih.gov/19822228

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant Bmp signaling and notochord delamination in the pathogenesis of esophageal atresia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19822228

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.EJMG.2009.10.001

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

ResearchGate publication ID

0 references

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