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

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

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

http://www.wikidata.org/entity/Q24655057

about

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations Gastroesophageal reflux and congenital gastrointestinal malformations VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis Molecular implications of evolutionary differences in CHD double chromodomains.Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes Poisson versus logistic regression in a descriptive epidemiologic analysis of data from a Birth Defects Registry.Renal dysplasia characterized by prominent cartilaginous metaplasia lesions in VACTERL association: A case report.Management of esophageal atresia and tracheoesophageal fistula in North Queensland.Review of genetic factors in intestinal malrotation.Mutational analysis of NOG in esophageal atresia and tracheoesophageal fistula patients.Long-term outcomes of adults with features of VACTERL association.Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association Analysis of genitourinary anomalies in patients with VACTERL (Vertebral anomalies, Anal atresia, Cardiac malformations, Tracheo-Esophageal fistula, Renal anomalies, Limb abnormalities) association.Oesophageal atresia with tracheo-oesophageal fistula in a preterm neonate in Limbe, Cameroon: case report & brief literature review De novo deletion of chromosome 20q13.33 in a patient with tracheo-esophageal fistula, cardiac defects and genitourinary anomalies implicates GTPBP5 as a candidate gene.A patient with VACTERL association for caesarean delivery.Prevalence of esophageal atresia among 18 international birth defects surveillance programs 13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature review Respiratory Care of Infants and Children with Congenital Tracheo-Oesophageal Fistula and Oesophageal Atresia.Esophageal atresia associated with anorectal malformation: Is the outcome better after surgery in two stages in a limited resources scenario?VACTERL Association Etiology: The Impact of de novo and Rare Copy Number Variations Adriamycin-Induced Models of VACTERL Association.Considering the Embryopathogenesis of VACTERL Association Embryology of oesophageal atresia.Control of vertebrate development by MYC Prune Belly Syndrome Associated with Full Spectrum of VACTERL in a New Born 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 Simultaneous Single-staged Repair of Anorectal Malformation with Tracheoesophageal Fistula: Lessons Learned.Etiology of esophageal atresia and tracheoesophageal fistula: "mind the gap".Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorder.A new syndrome with overlapping features of Townes-brocks syndrome and single median maxillary central incisor syndrome.Esophageal atresia and malrotation: what association?The Genetics Journey: A Case Report of a Genetic Diagnosis Made 30 Years Later.Improving the rigour of VACTERL screening for neonates with anorectal malformations.Surveillance in Patients With Esophageal Atresia/Tracheoesophageal Fistula.Gastric Function in Children with Oesophageal Atresia and Tracheoesophageal Fistula Prevalence, characteristics, and survival of children with esophageal atresia: A 32-year population-based study including 1,417,724 consecutive newborns.VACTERL (vertebral anomalies, anal atresia or imperforate anus, cardiac anomalies, tracheoesophageal fistula, renal and limb defect) spectrum presenting with portal hypertension: a case report Foregut separation and tracheo-oesophageal malformations: the role of tracheal outgrowth, dorso-ventral patterning and programmed cell death.Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts.

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

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

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CHARGE syndrome: report of 47 cases and review

Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome

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

Familial syndromic esophageal atresia maps to 2p23-p24.

Control of pancreas and liver gene expression by HNF transcription factors

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