Disease: Tracheoesophageal fistula symphalangism
- 5.9 Mb microdeletion in chromosome band 17q22-q23.2 associated with tracheo-esophageal fistula and conductive hearing loss
- Clinical and genetic approach in the characterization of newborns with anorectal malformation
- Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype
- Esophageal atresia/tracheoesophageal fistula and proximal symphalangism in a patient with a NOG nonsense mutation
- Extending the scope of the VATER association: definition of the VATER syndrome
- Feingold syndrome
- Feingold syndrome: report of a new family and review
- Growth hormone deficiency, aortic dilation, and neurocognitive issues in Feingold syndrome 2
- How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?
- Imaging rounds #111. VATER association
- Independent effects of maternal age and birth order on the incidence of selected congenital malformations
- Occurrence of Esophageal Atresia With Tracheoesophageal Fistula in Siblings From Three-Generation Family Affected by Variable Expressivity <em>MYCN</em> Mutation: A Case Report
- Occurrence of Esophageal Atresia With Tracheoesophageal Fistula in Siblings From Three-Generation Family Affected by Variable Expressivity MYCN Mutation: A Case Report
- The expanded spectrum of limb anomalies in the VATER association
- The MMT syndrome (microcephaly, mesobrachyphalangy and tracheoesophageal fistula). The first case described in Spain and a review of the literature
- Tracheoesophageal fistula, protruding pinnae, proximal interphalangeal symphalangism of fifth finger. A new syndrome?
- Urogenital sinus, rectovaginal fistula, and an anterior stenosed anus--another cloacal variant