BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

537 related articles for article (PubMed ID: 19296933)

  • 1. VATER/VACTERL syndrome (vertebra/anus/cardiac/trachea/esophogus/radius/renal/limb anomalies) with a noncommunicating functioning uterine horn and a unicornuate uterus: a case report.
    Nunes N; Karandikar S; Cooper S; Jaganathan R; Irani S
    Fertil Steril; 2009 May; 91(5):1957.e11-2. PubMed ID: 19296933
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Unicornuate uterus with a rudimentary non-communicating cavitary horn in association with VACTERL association: case report.
    Obeidat RA; Aleshawi AJ; Tashtush NA; Alsarawi H
    BMC Womens Health; 2019 May; 19(1):71. PubMed ID: 31146728
    [TBL] [Abstract][Full Text] [Related]  

  • 3. VACTERL association with a rare vertebral anomaly (butterfly vertebra) in a case of monochorionic twin.
    Sandal G; Aslan N; Duman L; Ormeci AR
    Genet Couns; 2014; 25(2):231-5. PubMed ID: 25059024
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Congenital anal atresia with rectovestibular fistula, scoliosis, unilateral renal agenesis, and finger defect (VACTERL association) in a patient with partial bicornuate uterus and distal vaginal atresia: A case report.
    Kang J; Mao M; Zhang Y; Ai FF; Zhu L
    Medicine (Baltimore); 2018 Nov; 97(45):e12822. PubMed ID: 30407282
    [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. 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]  

  • 8. 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]  

  • 9. VACTERL-association.
    Czeizel A; Ludányi I
    Acta Morphol Hung; 1984; 32(2):75-96. PubMed ID: 6435405
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. VACTERL (vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, cardiac defects, renal and limb anomalies) association: disease spectrum in 25 patients ascertained for their upper limb involvement.
    Carli D; Garagnani L; Lando M; Fairplay T; Bernasconi S; Landi A; Percesepe A
    J Pediatr; 2014 Mar; 164(3):458-62.e1-2. PubMed ID: 24210691
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Aberrant abdominal umbilical arteries in VACTERL--association: a first case report.
    Peonim V; Sujirachato K; Udnoon J; Chudoung U; Wongwichai S
    J Med Assoc Thai; 2012 Oct; 95(10):1352-6. PubMed ID: 23193752
    [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. 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]  

  • 15. VACTERL Association.
    Pandey DB; Pednekar SJ; Chavan SA; Korivi D; Shah AK; Kulkarni UP
    J Assoc Physicians India; 2011 Jul; 59():447-9. PubMed ID: 22315751
    [TBL] [Abstract][Full Text] [Related]  

  • 16. VACTERL/VATER Association.
    Solomon BD
    Orphanet J Rare Dis; 2011 Aug; 6():56. PubMed ID: 21846383
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lumbocostovertebral syndrome with associated VACTERL anomaly.
    Lyngdoh TS; Mahalik S; Naredi B; Samujh R; Khanna S
    J Pediatr Surg; 2010 Sep; 45(9):e15-7. PubMed ID: 20850610
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Adriamycin produces a reproducible teratogenic model of vertebral, anal, cardiovascular, tracheal, esophageal, renal, and limb anomalies in the mouse.
    Dawrant MJ; Giles S; Bannigan J; Puri P
    J Pediatr Surg; 2007 Oct; 42(10):1652-8. PubMed ID: 17923191
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. The etiology of VACTERL association: Current knowledge and hypotheses.
    Solomon BD
    Am J Med Genet C Semin Med Genet; 2018 Dec; 178(4):440-446. PubMed ID: 30580478
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 27.