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There are 17100 results for: content related to: Elements of morphology: Standard terminology for the periorbital region

  1. You have free access to this content

    Annals of Eugenics

    Volume 1, Issue 2, October 1925, Pages: 128–138, C. H. USHER

    Version of Record online : 13 APR 2011, DOI: 10.1111/j.1469-1809.1925.tb02039.x

  2. The epicanthus or Mongolian fold in Caucasian children

    American Journal of Physical Anthropology

    Volume 13, Issue 2, July/September 1929, Pages: 255–279, K. S. Chouke

    Version of Record online : 7 JUN 2005, DOI: 10.1002/ajpa.1330130224

  3. Wisconsin syndrome in a patient with interstitial deletion of the long arm of chromosome 3: Further delineation of the phenotype

    American Journal of Medical Genetics Part A

    Volume 120A, Issue 3, 30 July 2003, Pages: 413–417, Wai-tai Ko, Wai-fan Lam, Fai-man Lo, Wing-kwong Chan and Tak-sum Lam

    Version of Record online : 11 APR 2003, DOI: 10.1002/ajmg.a.20149

  4. Comparison of mongoloid and normal newborns

    Acta Paediatrica

    Volume 53, Issue S154, July 1964, Pages: 22–56,

    Version of Record online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1964.tb05146.x

  5. Measurement of tear production in black-tufted marmosets (Callithrix penicillata) using three different methods: modified Schirmer’s I, phenol red thread and standardized endodontic absorbent paper points

    Veterinary Ophthalmology

    Volume 15, Issue 6, November 2012, Pages: 376–382, Rogério R. Lange, Leandro Lima and Fabiano Montiani-Ferreira

    Version of Record online : 20 FEB 2012, DOI: 10.1111/j.1463-5224.2012.00998.x

  6. New perspectives on the face in fetal alcohol syndrome: What anthropometry tells us

    American Journal of Medical Genetics

    Volume 109, Issue 4, 15 May 2002, Pages: 249–260, Elizabeth S. Moore, Richard E. Ward, Paul L. Jamison, Colleen A. Morris, Patricia I. Bader and Bryan D. Hall

    Version of Record online : 26 MAR 2002, DOI: 10.1002/ajmg.10197

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    Analysis of FOXL2 detects three novel mutations and an atypical phenotype of blepharophimosis-ptosis-epicanthus inversus syndrome

    Clinical & Experimental Ophthalmology

    Volume 44, Issue 9, December 2016, Pages: 757–762, Anna Krepelova, Martina Simandlova, Marketa Vlckova, Pavel Kuthan, Andrea L Vincent and Petra Liskova

    Version of Record online : 1 JUL 2016, DOI: 10.1111/ceo.12783

  8. Neuroimaging Findings in Pediatric Genetic Skeletal Disorders: A Review

    Journal of Neuroimaging

    Volume 27, Issue 2, March/April 2017, Pages: 162–209, Matthias W. Wagner, Andrea Poretti, Jane E. Benson and Thierry A. G. M. Huisman

    Version of Record online : 21 DEC 2016, DOI: 10.1111/jon.12413

  9. 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

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    Michels syndrome, Carnevale syndrome, OSA syndrome, and Malpuech syndrome: Variable expression of a single disorder (3MC syndrome)?

    American Journal of Medical Genetics Part A

    Volume 137A, Issue 3, 1 September 2005, Pages: 332–335, Luigi Titomanlio, Selim Bennaceur, Dominique Bremond-Gignac, Clarisse Baumann, Olivier Dupuy and Alain Verloes

    Version of Record online : 11 AUG 2005, DOI: 10.1002/ajmg.a.30878

  11. Interstitial deletion in 3q in a patient with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: Clinical report and review of the literature

    American Journal of Medical Genetics Part A

    Volume 137A, Issue 1, 15 August 2005, Pages: 81–87, M.H. de Ru, J.J.P. Gille, A.W.M. Nieuwint, J.B. Bijlsma, J.F. van der Blij and J.M. van Hagen

    Version of Record online : 13 JUL 2005, DOI: 10.1002/ajmg.a.30786

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    The effect of vertical gaze position on ocular tear film stability

    Clinical and Experimental Optometry

    Volume 90, Issue 3, May 2007, Pages: 176–181, Tony Pansell, Madeleine Porsblad and Saber Abdi

    Version of Record online : 11 APR 2007, DOI: 10.1111/j.1444-0938.2007.00136.x

  13. Unraveling molecular pathways shared by Kabuki and Kabuki-like syndromes

    Clinical Genetics

    C. Lintas and A.M. Persico

    Version of Record online : 1 MAR 2017, DOI: 10.1111/cge.12983

  14. Anatomic Properties of the Upper Eyelid in Asian Americans

    Dermatologic Surgery

    Volume 35, Issue 11, November 2009, Pages: 1736–1740, MINHEE CHO and IOANNIS P. GLAVAS

    Version of Record online : 29 JUL 2009, DOI: 10.1111/j.1524-4725.2009.01285.x

  15. Del(18)(q12.2q21.1) caused by a paternal sister chromatid rearrangement in a developmentally delayed girl

    American Journal of Medical Genetics Part A

    Volume 135A, Issue 3, 15 June 2005, Pages: 304–307, Dieter Kotzot, Edda Haberlandt, Christine Fauth, Sara Baumgartner, Sabine Scholl-Bürgi and Gerd Utermann

    Version of Record online : 10 MAY 2005, DOI: 10.1002/ajmg.a.30727

  16. Fronto-otopalatodigital osteodysplasia: Clinical evidence for a single entity encompassing Melnick-Needles syndrome, otopalatodigital syndrome types 1 and 2, and frontometaphyseal dysplasia

    American Journal of Medical Genetics

    Volume 90, Issue 5, 28 February 2000, Pages: 407–422, Alain Verloes, Sylviane Lesenfants, Mason Barr, Dorothy K. Grange, Hubert Journel, Jacques Lombet, Gert Mortier and Elisabeth Roeder

    Version of Record online : 23 MAR 2000, DOI: 10.1002/(SICI)1096-8628(20000228)90:5<407::AID-AJMG11>3.0.CO;2-D

  17. Three additional cases of the Michels syndrome

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 22, 15 November 2007, Pages: 2747–2750, Gabriela F. Leal and Eduardo V.P. Baptista

    Version of Record online : 15 OCT 2007, DOI: 10.1002/ajmg.a.32029

  18. ADAT3-related intellectual disability: Further delineation of the phenotype

    American Journal of Medical Genetics Part A

    Volume 170, Issue 5, May 2016, Pages: 1142–1147, Ayman W. El-Hattab, Mohammed A. Saleh, Amal Hashem, Mohammed Al-Owain, Ali Al Asmari, Hala Rabei, Hanem Abdelraouf, Mais Hashem, Anas M. Alazami, Nisha Patel, Ranad Shaheen, Eissa A. Faqeih and Fowzan S. Alkuraya

    Version of Record online : 3 FEB 2016, DOI: 10.1002/ajmg.a.37578


    Acta Ophthalmologica

    Volume 61, Issue 1, February 1983, Pages: 108–116, JEFFREY P. GILBARD and R. LINSY FARRIS

    Version of Record online : 27 MAY 2009, DOI: 10.1111/j.1755-3768.1983.tb01401.x

  20. Blepharophimosis-mental retardation (BMR) syndromes: A proposed clinical classification of the so-called Ohdo syndrome, and delineation of two new BMR syndromes, one X-linked and one autosomal recessive

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 12, 15 June 2006, Pages: 1285–1296, Alain Verloes, Dominique Bremond-Gignac, Bertrand Isidor, Albert David, Clarisse Baumann, Marie-Anne Leroy, René Stevens, Yves Gillerot, Delphine Héron, Bénédicte Héron, Brigitte Benzacken, Didier Lacombe, Han Brunner and Pierre Bitoun

    Version of Record online : 12 MAY 2006, DOI: 10.1002/ajmg.a.31270