282 related articles for article (PubMed ID: 19822228)
1. 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.
Shaw-Smith C
Eur J Med Genet; 2010; 53(1):6-13. PubMed ID: 19822228
[TBL] [Abstract][Full Text] [Related]
2. Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association.
Agochukwu NB; Pineda-Alvarez DE; Keaton AA; Warren-Mora N; Raam MS; Kamat A; Chandrasekharappa SC; Solomon BD
Eur J Med Genet; 2011; 54(3):323-8. PubMed ID: 21315191
[TBL] [Abstract][Full Text] [Related]
3. Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology.
Shaw-Smith C
J Med Genet; 2006 Jul; 43(7):545-54. PubMed ID: 16299066
[TBL] [Abstract][Full Text] [Related]
4. Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia.
Ranza E; Le Gouez M; Guimier A; Dunlop NK; Beaudoin S; Malan V; Michot C; Baujat G; Rio M; Cormier-Daire V; Abadie V; Sarnacki S; Delacourt C; Lyonnet S; Attié-Bitach T; Pingault V; Rousseau V; Amiel J
Am J Med Genet A; 2023 Jan; 191(1):77-83. PubMed ID: 36271508
[TBL] [Abstract][Full Text] [Related]
5. Identification of a HOXD13 mutation in a VACTERL patient.
Garcia-Barceló MM; Wong KK; Lui VC; Yuan ZW; So MT; Ngan ES; Miao XP; Chung PH; Khong PL; Tam PK
Am J Med Genet A; 2008 Dec; 146A(24):3181-5. PubMed ID: 19006232
[TBL] [Abstract][Full Text] [Related]
6. Patterns of malformation associated with esophageal atresia/tracheoesophageal fistula: A retrospective single center study.
Galarreta CI; Vaida F; Bird LM
Am J Med Genet A; 2020 Jun; 182(6):1351-1363. PubMed ID: 32250545
[TBL] [Abstract][Full Text] [Related]
7. Non-VACTERL-type anomalies are frequent in patients with esophageal atresia/tracheo-esophageal fistula and full or partial VACTERL association.
de Jong EM; Felix JF; Deurloo JA; van Dooren MF; Aronson DC; Torfs CP; Heij HA; Tibboel D
Birth Defects Res A Clin Mol Teratol; 2008 Feb; 82(2):92-7. PubMed ID: 18186125
[TBL] [Abstract][Full Text] [Related]
8. Accompanied anomalies in anal atresia or tracheo-esophageal fistula: Comparison with or without VACTERL association.
Ahn JH; Choi HJ
Birth Defects Res; 2021 May; 113(9):696-701. PubMed ID: 33616304
[TBL] [Abstract][Full Text] [Related]
9. Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.
Stankiewicz P; Sen P; Bhatt SS; Storer M; Xia Z; Bejjani BA; Ou Z; Wiszniewska J; Driscoll DJ; Maisenbacher MK; Bolivar J; Bauer M; Zackai EH; McDonald-McGinn D; Nowaczyk MM; Murray M; Hustead V; Mascotti K; Schultz R; Hallam L; McRae D; Nicholson AG; Newbury R; Durham-O'Donnell J; Knight G; Kini U; Shaikh TH; Martin V; Tyreman M; Simonic I; Willatt L; Paterson J; Mehta S; Rajan D; Fitzgerald T; Gribble S; Prigmore E; Patel A; Shaffer LG; Carter NP; Cheung SW; Langston C; Shaw-Smith C
Am J Hum Genet; 2009 Jun; 84(6):780-91. PubMed ID: 19500772
[TBL] [Abstract][Full Text] [Related]
10. Clinical and etiological heterogeneity in patients with tracheo-esophageal malformations and associated anomalies.
Brosens E; Ploeg M; van Bever Y; Koopmans AE; IJsselstijn H; Rottier RJ; Wijnen R; Tibboel D; de Klein A
Eur J Med Genet; 2014 Aug; 57(8):440-52. PubMed ID: 24931924
[TBL] [Abstract][Full Text] [Related]
11. VACTERL associations in children undergoing surgery for esophageal atresia and anorectal malformations: Implications for pediatric surgeons.
Lautz TB; Mandelia A; Radhakrishnan J
J Pediatr Surg; 2015 Aug; 50(8):1245-50. PubMed ID: 25913268
[TBL] [Abstract][Full Text] [Related]
12. Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: no evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrum.
Choinitzki V; Zwink N; Bartels E; Baudisch F; Boemers TM; Hölscher A; Turial S; Bachour H; Heydweiller A; Kurz R; Bartmann P; Pauly M; Brokmeier U; Leutner A; Nöthen MM; Schumacher J; Jenetzky E; Reutter H
Birth Defects Res A Clin Mol Teratol; 2013 Dec; 97(12):786-91. PubMed ID: 24307608
[TBL] [Abstract][Full Text] [Related]
13. Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association.
Hilger AC; Halbritter J; Pennimpede T; van der Ven A; Sarma G; Braun DA; Porath JD; Kohl S; Hwang DY; Dworschak GC; Hermann BG; Pavlova A; El-Maarri O; Nöthen MM; Ludwig M; Reutter H; Hildebrandt F
Hum Mutat; 2015 Dec; 36(12):1150-4. PubMed ID: 26294094
[TBL] [Abstract][Full Text] [Related]
14. Esophageal atresia with tracheoesophageal fistula in a patient with 7q35-36.3 deletion including SHH gene.
Busa T; Panait N; Chaumoitre K; Philip N; Missirian C
Eur J Med Genet; 2016 Oct; 59(10):546-8. PubMed ID: 27614115
[TBL] [Abstract][Full Text] [Related]
15. Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotype.
Reutter H; Hilger AC; Hildebrandt F; Ludwig M
Pediatr Nephrol; 2016 Nov; 31(11):2025-33. PubMed ID: 26857713
[TBL] [Abstract][Full Text] [Related]
16. Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genes.
Kolvenbach CM; van der Ven AT; Kause F; Shril S; Scala M; Connaughton DM; Mann N; Nakayama M; Dai R; Kitzler TM; Schneider R; Schierbaum L; Schneider S; Accogli A; Torella A; Piatelli G; Nigro V; Capra V; Hoppe B; Märzheuser S; Schmiedeke E; Rehm HL; Mane S; Lifton RP; Dworschak GC; Hilger AC; Reutter H; Hildebrandt F
Am J Med Genet A; 2021 Dec; 185(12):3784-3792. PubMed ID: 34338422
[TBL] [Abstract][Full Text] [Related]
17. [Vater or Vacterl syndrome (author's transl)].
Baumann W; Greinacher I; Emmrich P; Spranger J
Klin Padiatr; 1976 Jul; 188(4):328-37. PubMed ID: 988425
[TBL] [Abstract][Full Text] [Related]
18. Report of a girl with vacterl syndrome and right pulmonary agenesis.
Avcu S; Akgun C; Temel H; Arslan S; Akbayram S; Unal O
Genet Couns; 2009; 20(4):379-83. PubMed ID: 20162874
[TBL] [Abstract][Full Text] [Related]
19. Sonic hedgehog mutation analysis in patients with VACTERL association.
Aguinaga M; Zenteno JC; Pérez-Cano H; Morán V
Am J Med Genet A; 2010 Mar; 152A(3):781-3. PubMed ID: 20186790
[No Abstract] [Full Text] [Related]
20. Visualizing expression patterns of Shh and Foxf1 genes in the foregut and lung buds by optical projection tomography.
Sato H; Murphy P; Giles S; Bannigan J; Takayasu H; Puri P
Pediatr Surg Int; 2008 Jan; 24(1):3-11. PubMed ID: 17962963
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]