These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 20186795)

  • 1. VACTERL association in a cat.
    Moura E; Cirio SM; Villanova JA
    Am J Med Genet A; 2010 Mar; 152A(3):777-80. PubMed ID: 20186795
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association.
    Hilger A; Schramm C; Pennimpede T; Wittler L; Dworschak GC; Bartels E; Engels H; Zink AM; Degenhardt F; Müller AM; Schmiedeke E; Grasshoff-Derr S; Märzheuser S; Hosie S; Holland-Cunz S; Wijers CH; Marcelis CL; van Rooij IA; Hildebrandt F; Herrmann BG; Nöthen MM; Ludwig M; Reutter H; Draaken M
    Eur J Hum Genet; 2013 Dec; 21(12):1377-82. PubMed ID: 23549274
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial occurrence of the VATER/VACTERL association.
    Hilger A; Schramm C; Draaken M; Mughal SS; Dworschak G; Bartels E; Hoffmann P; Nöthen MM; Reutter H; Ludwig M
    Pediatr Surg Int; 2012 Jul; 28(7):725-9. PubMed ID: 22422375
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.
    Zhang R; Marsch F; Kause F; Degenhardt F; Schmiedeke E; Märzheuser S; Hoppe B; Bachour H; Boemers TM; Schäfer M; Spychalski N; Neser J; Leonhardt J; Kosch F; Ure B; Gómez B; Lacher M; Deffaa OJ; Palta M; Wittekindt B; Kleine K; Schmedding A; Grasshoff-Derr S; Ven AV; Heilmann-Heimbach S; Zwink N; Jenetzky E; Ludwig M; Reutter H
    Birth Defects Res; 2017 Jul; 109(13):1063-1069. PubMed ID: 28605140
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in PTF1A are not a common cause for human VATER/VACTERL association or neural tube defects mirroring Danforth's short tail mouse.
    Gurung N; Grosse G; Draaken M; Hilger AC; Nauman N; Müller A; Gembruch U; Merz WM; Reutter H; Ludwig M
    Mol Med Rep; 2015 Jul; 12(1):1579-83. PubMed ID: 25775927
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. VATER/VACTERL Association and Caudal Regression with Xq25-q27.3 Microdeletion: A Case Report.
    Puvabanditsin S; Van Gurp J; February M; Khalil M; Mayne J; Ai McConnell J; Mehta R
    Fetal Pediatr Pathol; 2016; 35(2):133-41. PubMed ID: 26881326
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [Etiopathogenetic study of the VACTERL association].
    Ludányi I; Czeizel E
    Orv Hetil; 1984 Apr; 125(14):825-9. PubMed ID: 6709346
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL-like association and analysis of EFNB2 in patients with anorectal malformations.
    Dworschak GC; Draaken M; Marcelis C; de Blaauw I; Pfundt R; van Rooij IA; Bartels E; Hilger A; Jenetzky E; Schmiedeke E; Grasshoff-Derr S; Schmidt D; Märzheuser S; Hosie S; Weih S; Holland-Cunz S; Palta M; Leonhardt J; Schäfer M; Kujath C; Rissmann A; Nöthen MM; Zwink N; Ludwig M; Reutter H
    Am J Med Genet A; 2013 Dec; 161A(12):3035-41. PubMed ID: 24038947
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Bilateral ureteral triplication with crossed ectopic fused kidneys associated with the VACTERL syndrome.
    Golomb J; Ehrlich RM
    J Urol; 1989 Jun; 141(6):1398-9. PubMed ID: 2657108
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.
    Zeidler C; Woelfle J; Draaken M; Mughal SS; Große G; Hilger AC; Dworschak GC; Boemers TM; Jenetzky E; Zwink N; Lacher M; Schmidt D; Schmiedeke E; Grasshoff-Derr S; Märzheuser S; Holland-Cunz S; Schäfer M; Bartels E; Keppler K; Palta M; Leonhardt J; Kujath C; Rißmann A; Nöthen MM; Reutter H; Ludwig M
    Birth Defects Res A Clin Mol Teratol; 2014 Oct; 100(10):750-9. PubMed ID: 25131394
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Bronchial anomalies in VACTERL association.
    Kanu A; Tegay D; Scriven R
    Pediatr Pulmonol; 2008 Sep; 43(9):930-2. PubMed ID: 18671276
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evidence for annular pancreas as an associated anomaly in the VATER/VACTERL association and investigation of the gene encoding pancreas specific transcription factor 1A as a candidate gene.
    Reutter H; Gurung N; Ludwig M
    Am J Med Genet A; 2014 Jun; 164A(6):1611-3. PubMed ID: 24668915
    [No Abstract]   [Full Text] [Related]  

  • 18. VACTERL as primary, polytopic developmental field defects.
    Martínez-Frías ML; Frías JL
    Am J Med Genet; 1999 Mar; 83(1):13-6. PubMed ID: 10076879
    [TBL] [Abstract][Full Text] [Related]  

  • 19. X-linked VACTERL with hydrocephalus: the VACTERL-H syndrome.
    Genuardi M; Chiurazzi P; Capelli A; Neri G
    Birth Defects Orig Artic Ser; 1993; 29(1):235-41. PubMed ID: 8280876
    [No Abstract]   [Full Text] [Related]  

  • 20. The VATER association. Vertebral defects, Anal atresia, T-E fistula with esophageal atresia, Radial and Renal dysplasia: a spectrum of associated defects.
    Quan L; Smith DW
    J Pediatr; 1973 Jan; 82(1):104-7. PubMed ID: 4681850
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.