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There are 31198 results for: content related to: A maneuver to assess the presence of metacarpal or metatarsal osseous syndactyly: A physical finding useful for the differential diagnosis of polydactyly

  1. You have free access to this content
    Elements of morphology: Standard terminology for the hands and feet

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 1, January 2009, Pages: 93–127, Leslie G. Biesecker, Jon M. Aase, Carol Clericuzio, Fiorella Gurrieri, I. Karen Temple and Helga Toriello

    Version of Record online : 5 JAN 2009, DOI: 10.1002/ajmg.a.32596

    Corrected by:

    Corrigendum: Corrigendum to “Elements of Morphology: Standard Terminology for the Hands and Feet. Am J Med Genet 2009 149A:93–127”

    Vol. 158A, Issue 7, 1813, Version of Record online: 18 JUN 2012

  2. Polydactyly: phenotypes, genetics and classification

    Clinical Genetics

    Volume 85, Issue 3, March 2014, Pages: 203–212, S. Malik

    Version of Record online : 18 OCT 2013, DOI: 10.1111/cge.12276

  3. Familial crossed polysyndactyly

    American Journal of Medical Genetics

    Volume 50, Issue 3, 15 April 1994, Pages: 215–223, David J. Goldstein, Marios Kambouris and Richard E. Ward

    Version of Record online : 7 JUN 2005, DOI: 10.1002/ajmg.1320500302

  4. A 72-year-old Danish puzzle resolved—comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansions

    American Journal of Medical Genetics Part A

    Volume 138A, Issue 4, 1 November 2005, Pages: 328–339, Klaus W. Kjaer, Lars Hansen, Hans Eiberg, Algirdas Utkus, Lene T. Skovgaard, Pernille Leicht, John M. Opitz and Niels Tommerup

    Version of Record online : 12 OCT 2005, DOI: 10.1002/ajmg.a.30971

  5. Are triphalangeal thumb-polysyndactyly syndrome (TPTPS) and tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome (THPTTS) identical? A father with TPTPS and his daughter with THPTTS in a Thai family

    American Journal of Medical Genetics

    Volume 93, Issue 2, 17 July 2000, Pages: 126–131, Piranit N. Kantaputra and Preecha Chalidapong

    Version of Record online : 21 JUN 2000, DOI: 10.1002/1096-8628(20000717)93:2<126::AID-AJMG9>3.0.CO;2-S

  6. The clinical atlas of Greig cephalopolysyndactyly syndrome

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 5, 1 March 2008, Pages: 548–557, Katherine Balk and Leslie G. Biesecker

    Version of Record online : 1 FEB 2008, DOI: 10.1002/ajmg.a.32167

  7. Associated anomalies in individuals with polydactyly

    American Journal of Medical Genetics

    Volume 80, Issue 5, 28 December 1998, Pages: 459–465, Eduardo E. Castilla, Regina Lugarinho, Maria da Graça Dutra and Leonardo J. Salgado

    Version of Record online : 29 JAN 1999, DOI: 10.1002/(SICI)1096-8628(19981228)80:5<459::AID-AJMG5>3.0.CO;2-G

  8. Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly—a new syndrome? Part I: Clinical, causal, and pathogenetic considerations

    American Journal of Medical Genetics

    Volume 7, Issue 1, 1980, Pages: 47–74, Dr. J. G. Hall, P. D. Pallister, S. K. Clarren, J. B. Beckwith, F. W. Wiglesworth, F. C. Fraser, S. Cho, P. J. Benke, S. D. Reed and John M. Optiz

    Version of Record online : 3 JUN 2005, DOI: 10.1002/ajmg.1320070110

  9. Skeletal Dysplasias: Defects in Skeletal Morphogenesis

    Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects, Second Edition

    Stefan Mundlos, Bjorn R. Olsen, Pages: 993–1023, 2003

    Published Online : 30 APR 2003, DOI: 10.1002/0471221929.ch23(v)

  10. An infant with large fontanelles, aplasia cutis congenita, tessier facial cleft, polydactyly inversus, and toe syndactyly: A previously undescribed syndrome?

    American Journal of Medical Genetics Part A

    Volume 167, Issue 4, April 2015, Pages: 683–687, Jessica Jackson, Paula Delk, Emily Farrow, Christopher Griffith, Melissa Lah and David D. Weaver

    Version of Record online : 23 FEB 2015, DOI: 10.1002/ajmg.a.36927

  11. Mesoaxial polydactyly is a major feature in Bardet–Biedl syndrome patients with LZTFL1 (BBS17) mutations

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 476–481, E. Schaefer, J. Lauer, M. Durand, V. Pelletier, C. Obringer, A. Claussmann, J.-J. Braun, C. Redin, C. Mathis, J. Muller, C. Schmidt-Mutter, E. Flori, V. Marion, C. Stoetzel and H. Dollfus

    Version of Record online : 12 JUN 2013, DOI: 10.1111/cge.12198

  12. You have free access to this content

    Annals of Eugenics

    Volume 12, Issue 1, January 1943, Pages: 220–249, S. B. HOLT

    Version of Record online : 13 APR 2011, DOI: 10.1111/j.1469-1809.1943.tb02326.x

  13. Genetic heterogeneity in type III familial cutaneous syndactyly and linkage to chromosome 7q36

    American Journal of Medical Genetics Part A

    Volume 161, Issue 7, July 2013, Pages: 1579–1584, Mohammad M. Al-Qattan, Hanan E. Shamseldin, Mohammed Al Mazyad, Saud Al Deghaither and Fowzan S. Alkuraya

    Version of Record online : 17 MAY 2013, DOI: 10.1002/ajmg.a.35956

  14. Fetal Skeletal Anomalies

    Clinical Obstetrics: The Fetus & Mother, Third Edition

    Luís F. Gonçalves, Patricia L. Devers, Jimmy Espinoza, Roberto Romero, Pages: 401–472, 2008

    Published Online : 14 JAN 2008, DOI: 10.1002/9780470753293.ch26

  15. Molecular analysis of non-syndromic preaxial polydactyly: preaxial polydactyly type-IV and preaxial polydactyly type-I

    Clinical Genetics

    Volume 67, Issue 5, May 2005, Pages: 429–433, H Fujioka, T Ariga, K Horiuchi, M Otsu, H Igawa, K Kawashima, Y Yamamoto, T Sugihara and Y Sakiyama

    Version of Record online : 10 MAR 2005, DOI: 10.1111/j.1399-0004.2005.00431.x

  16. Atypical crossed polydactyly in two siblings with Ellis-van Creveld Syndrome and mild clinical manifestations in close relatives

    Pediatrics International

    Volume 46, Issue 2, April 2004, Pages: 184–187, Aysenur Ökten, Murat Çakir, Fazil Orhan and Ilke Mungan

    Version of Record online : 5 APR 2004, DOI: 10.1046/j.1442-200x.2004.01871.x

  17. 35th Annual David W Smith Workshop on Malformations and Morphogenesis: Abstracts of the 2014 Annual Meeting

    American Journal of Medical Genetics Part A

    Volume 167, Issue 8, August 2015, Pages: 1685–1740, Stephen R. Braddock, Robert J. Lipinski, Marc S. Williams and John C. Carey

    Version of Record online : 22 MAY 2015, DOI: 10.1002/ajmg.a.37107

  18. You have free access to this content
    Polydactyly: How many disorders and how many genes? 2010 update

    Developmental Dynamics

    Volume 240, Issue 5, May 2011, Pages: 931–942, Leslie G. Biesecker

    Version of Record online : 28 MAR 2011, DOI: 10.1002/dvdy.22609

  19. A novel mutation (g.106737G>T) in zone of polarizing activity regulatory sequence (ZRS) causes variable limb phenotypes in Werner mesomelia

    American Journal of Medical Genetics Part A

    Volume 164, Issue 4, April 2014, Pages: 898–906, Katta M. Girisha, Abdul Mueed Bidchol, Preeti S. Kamath, Krupa H. Shah, Geert R. Mortier, Stefan Mundlos and Hitesh Shah

    Version of Record online : 29 JAN 2014, DOI: 10.1002/ajmg.a.36367

  20. Polydactyly in the prehistoric American Southwest

    International Journal of Osteoarchaeology

    Volume 16, Issue 3, May/June 2006, Pages: 221–235, D. T. Case, R. J. Hill, C. F. Merbs and M. Fong

    Version of Record online : 22 MAY 2006, DOI: 10.1002/oa.820