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There are 9097 results for: content related to: Clinical geneticists' views of VACTERL/VATER association

  1. Anorectal anomalies associated with or as part of other anomalies

    American Journal of Medical Genetics

    Volume 110, Issue 2, 15 June 2002, Pages: 122–130, Alfred Cuschieri

    Version of Record online : 16 APR 2002, DOI: 10.1002/ajmg.10371

  2. 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

  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. 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

  5. You have free access to this content
    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

  6. 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

  7. 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

  8. 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

  9. 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

  10. 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

  11. You have free access to this content
    Monochorionic twin fetus with VACTERL association after intracytoplasmic sperm injection

    Congenital Anomalies

    Volume 53, Issue 2, June 2013, Pages: 95–97, Tomonobu Kanasugi, Akihiko Kikuchi, Atsushi Matsumoto, Miyuki Terata, Chizuko Isurugi, Rie Oyama, Akimune Fukushima and Toru Sugiyama

    Version of Record online : 10 JUN 2013, DOI: 10.1111/j.1741-4520.2012.00373.x

  12. Beyond Gómez-López-Hernández syndrome: Recurring phenotypic themes in rhombencephalosynapsis

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 10, October 2012, Pages: 2393–2406, Hannah M. Tully, Jennifer C. Dempsey, Gisele E. Ishak, Margaret P. Adam, Cynthia J.R. Curry, Pedro Sanchez-Lara, Alasdair Hunter, Karen W. Gripp, Judith Allanson, Christopher Cunniff, Ian Glass, Kathleen J. Millen, Daniel Doherty and William B. Dobyns

    Version of Record online : 10 SEP 2012, DOI: 10.1002/ajmg.a.35561

  13. 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

  14. Contribution of LPP copy number and sequence changes to esophageal atresia, tracheoesophageal fistula, and VACTERL association

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 7, July 2012, Pages: 1785–1787, Andrés Hernández-García, Erwin Brosens, Hitisha P. Zaveri, Elisabeth M. de Jong, Zhiyin Yu, Maria Namwanje, Allison Mayle, Caraciolo J. Fernandes, Brendan Lee, Maria Blazo, Seema R. Lalani, Dick Tibboel, Annelies de Klein and Daryl A. Scott

    Version of Record online : 25 MAY 2012, DOI: 10.1002/ajmg.a.35391

  15. 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

  16. Familial recurrence of tracheoesophageal fistula and associated malformations

    American Journal of Medical Genetics

    Volume 63, Issue 4, 28 June 1996, Pages: 525–528, Kevin P. McMullen, Pamela S. Karnes, Christopher R. Moir and Virginia V. Michels

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19960628)63:4<525::AID-AJMG3>3.0.CO;2-N

  17. Distal 13q Deletion Syndrome and the VACTERL Association: Case report, literature review, and possible implications

    American Journal of Medical Genetics

    Volume 98, Issue 2, 15 January 2001, Pages: 137–144, Laurence E. Walsh, Gail H. Vance and David D. Weaver

    Version of Record online : 28 DEC 2000, DOI: 10.1002/1096-8628(20010115)98:2<137::AID-AJMG1022>3.0.CO;2-5

  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. 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

  20. VACTERL with hydrocephalus: Further delineation of the syndrome(s)

    American Journal of Medical Genetics

    Volume 34, Issue 2, October 1989, Pages: 177–182, Dr. Jane A. Evans, Leonie C. Stranc, Paige Kaplan and Alasdair G. W. Hunter

    Version of Record online : 5 JUN 2005, DOI: 10.1002/ajmg.1320340209