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There are 13457 results for: content related to: A rare association of fibromuscular dysplasia, renal agenesis, renal arteriovenous fistulae, and vertebral anomalies: Expanding the V in VACTERL association

  1. Analysis of genitourinary anomalies in patients with VACTERL (Vertebral anomalies, Anal atresia, Cardiac malformations, Tracheo-Esophageal fistula, Renal anomalies, Limb abnormalities) association

    Congenital Anomalies

    Volume 51, Issue 2, June 2011, Pages: 87–91, Benjamin D. Solomon, Manu S. Raam and Daniel E. Pineda-Alvarez

    Version of Record online : 20 MAY 2011, DOI: 10.1111/j.1741-4520.2010.00303.x

  2. Clinical characteristics of neonates With VACTERL association

    Pediatrics International

    Volume 54, Issue 3, June 2012, Pages: 361–364, Akgun Oral, Ibrahim Caner, Murat Yigiter, Mecit Kantarci, Hasim Olgun, Naci Ceviz and Ahmet Bedii Salman

    Version of Record online : 9 APR 2012, DOI: 10.1111/j.1442-200X.2012.03566.x

  3. Analysis of renal anomalies in VACTERL association

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 100, Issue 10, October 2014, Pages: 801–805, Bridget K. Cunningham, Alina Khromykh, Ariel F. Martinez, Tyler Carney, Donald W. Hadley and Benjamin D. Solomon

    Version of Record online : 5 SEP 2014, DOI: 10.1002/bdra.23302

  4. Congenital abnormalities associated with limb deficiency defects: A population study based on cases from the Hungarian congenital malformation registry (1975–1984)

    American Journal of Medical Genetics

    Volume 49, Issue 1, 1 January 1994, Pages: 52–66, Dr. J. A. Evans, M. Vitez and A. Czeizel

    Version of Record online : 7 JUN 2005, DOI: 10.1002/ajmg.1320490111

  5. Clinical geneticists' views of VACTERL/VATER association

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 12, December 2012, Pages: 3087–3100, Benjamin D. Solomon, Kelly A. Bear, Virginia Kimonis, Annelies de Klein, Daryl A. Scott, Charles Shaw-Smith, Dick Tibboel, Heiko Reutter and Philip F. Giampietro

    Version of Record online : 19 NOV 2012, DOI: 10.1002/ajmg.a.35638

  6. X-linked VACTERL with hydrocephalus syndrome: Further delineation of the phenotype caused by FANCB mutations

    American Journal of Medical Genetics Part A

    Volume 155, Issue 10, October 2011, Pages: 2370–2380, Joanna McCauley, Navta Masand, Ruth McGowan, Sulekha Rajagopalan, Alasdair Hunter, Jacques L. Michaud, Kate Gibson, Jeremy Robertson, Fiona Vaz, Stephen Abbs and Simon T. Holden

    Version of Record online : 9 SEP 2011, DOI: 10.1002/ajmg.a.33913

  7. Rib defects in patterns of multiple malformations: A retrospective review and phenotypic analysis of 47 cases

    American Journal of Medical Genetics Part A

    Volume 122A, Issue 1, 15 September 2003, Pages: 63–69, Duangrurdee Wattanasirichaigoon, Chitra Prasad, Gretchen Schneider, Jane A. Evans and Bruce R. Korf

    Version of Record online : 8 MAY 2003, DOI: 10.1002/ajmg.a.20241

  8. Prenatal diagnosis of the VACTERL association using routine ultrasound examination

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 103, Issue 10, October 2015, Pages: 880–886, Anne Debost-Legrand, Carole Goumy, Hélène Laurichesse-Delmas, Pierre Déchelotte, Isabelle Perthus, Christine Francannet, Didier Lémery and Denis Gallot

    Version of Record online : 2 JUN 2015, DOI: 10.1002/bdra.23346

  9. The VACTERL Association as a disturbance of cell fate determination

    American Journal of Medical Genetics Part A

    Volume 167, Issue 11, November 2015, Pages: 2582–2588, Mark Lubinsky

    Version of Record online : 14 JUL 2015, DOI: 10.1002/ajmg.a.37238

  10. Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC)

    American Journal of Medical Genetics Part A

    Volume 121A, Issue 2, 30 August 2003, Pages: 151–155, Carsten Bergmann, Klaus Zerres, Thomas Peschgens, Jan Senderek, Helmut Hörnchen and Sabine Rudnik-Schöneborn

    Version of Record online : 9 APR 2003, DOI: 10.1002/ajmg.a.20167

  11. Thinking of VACTERL-H? Rule out Fanconi Anemia according to PHENOS

    American Journal of Medical Genetics Part A

    Volume 170, Issue 6, June 2016, Pages: 1520–1524, Blanche P. Alter and Neelam Giri

    Version of Record online : 30 MAR 2016, DOI: 10.1002/ajmg.a.37637

  12. Patterns in multimalformed babies and the question of the relationship between sirenomelia and VACTERL

    American Journal of Medical Genetics

    Volume 49, Issue 1, 1 January 1994, Pages: 29–35, Lavínia Schüler and Francisco M. Salzano

    Version of Record online : 7 JUN 2005, DOI: 10.1002/ajmg.1320490108

  13. Sirenomelia: A new type, Showing VACTERL Association with thomas syndrome and a review of literature

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 97, Issue 3, March 2013, Pages: 123–132, Martin Lhuaire, Agnès Jestin, Camille Boulagnon, Mélanie Loock, Martine Doco-Fenzy, Dominique Gaillard, Marie-Danièle Diebold, Claude Avisse and Marc Labrousse

    Version of Record online : 23 MAR 2013, DOI: 10.1002/bdra.23125

    Corrected by:

    Erratum: Erratum

    Vol. 97, Issue 6, 429, Version of Record online: 13 JUN 2013

  14. Tibial developmental field defect is the most common lower limb malformation pattern in VACTERL association

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 10, 15 May 2008, Pages: 1259–1266, Marco Castori, Rosanna Rinaldi, Sandra Cappellacci and Paola Grammatico

    Version of Record online : 3 APR 2008, DOI: 10.1002/ajmg.a.32288

  15. VACTERL association, epidemiologic definition and delineation

    American Journal of Medical Genetics

    Volume 63, Issue 4, 28 June 1996, Pages: 529–536, Monica Rittler, Joaquin E. Paz and Eduardo E. Castilla

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19960628)63:4<529::AID-AJMG4>3.0.CO;2-J

  16. Should chromosome breakage studies be performed in patients with VACTERL association?

    American Journal of Medical Genetics Part A

    Volume 137A, Issue 1, 15 August 2005, Pages: 55–58, Laurence Faivre, Marie France Portnoï, Gerard Pals, Dominique Stoppa-Lyonnet, Martine Le Merrer, Christel Thauvin-Robinet, Frédéric Huet, Christopher G. Mathew, Hans Joenje, Alain Verloes and Clarisse Baumann

    Version of Record online : 13 JUL 2005, DOI: 10.1002/ajmg.a.30853

  17. Holoprosencephaly and limb reduction defects: A consideration of Steinfeld syndrome and related conditions

    American Journal of Medical Genetics Part A

    Volume 134A, Issue 4, 1 May 2005, Pages: 381–392, Joseph R. Siebert, Kelly A. Schoenecker, Robert G. Resta and Raj P. Kapur

    Version of Record online : 18 MAR 2005, DOI: 10.1002/ajmg.a.30648

  18. Sonic Hedgehog, VACTERL, and Fanconi anemia: Pathogenetic connections and therapeutic implications

    American Journal of Medical Genetics Part A

    Volume 167, Issue 11, November 2015, Pages: 2594–2598, Mark Lubinsky

    Version of Record online : 21 JUL 2015, DOI: 10.1002/ajmg.a.37257

  19. Non-VACTERL-type anomalies are frequent in patients with esophageal atresia/tracheo-esophageal fistula and full or partial VACTERL association

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 82, Issue 2, February 2008, Pages: 92–97, Elisabeth M. de Jong, Janine F. Felix, Jacqueline A. Deurloo, Marieke F. van Dooren, Daniël C. Aronson, Claudine P. Torfs, Hugo A. Heij and Dick Tibboel

    Version of Record online : 9 JAN 2008, DOI: 10.1002/bdra.20437

  20. Anesthesia for the Patient with a Genetic Syndrome

    Gregory's Pediatric Anesthesia, Fifth Edition

    David Mann, Priscilla J. Garcia, Dean B. Andropoulos, Pages: 993–1139, 2011

    Published Online : 9 DEC 2011, DOI: 10.1002/9781444345186.ch38