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There are 11094 results for: content related to: Large-scale objective phenotyping of 3D facial morphology

  1. 3D morphometry aids facial analysis of individuals with a childhood cancer

    American Journal of Medical Genetics Part A

    Volume 170, Issue 11, November 2016, Pages: 2905–2915, Saskia M. J. Hopman, Johannes H. M. Merks, Michael Suttie, Raoul C. M. Hennekam and Peter Hammond

    Version of Record online : 2 AUG 2016, DOI: 10.1002/ajmg.a.37850

  2. Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: Six new patients

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 504–511, Guillaume Jedraszak, Bénédicte Demeer, Michèle Mathieu-Dramard, Joris Andrieux, Aline Receveur, Astrid Weber, Una Maye, Nicola Foulds, IK Temple, John Crolla, Marie-Pierre Alex-Cordier, Damien Sanlaville, Lisa Ewans, Meredith Wilson, Ruth Armstrong, Amanda Clarkson, Henri Copin and Gilles Morin

    Version of Record online : 8 JAN 2015, DOI: 10.1002/ajmg.a.36882

  3. State birth defects surveillance program directory

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 70, Issue 9, September 2004, Pages: 609–676,

    Version of Record online : 7 SEP 2004, DOI: 10.1002/bdra.20071

  4. Facial Curvature Detects and Explicates Ethnic Differences in Effects of Prenatal Alcohol Exposure

    Alcoholism: Clinical and Experimental Research

    Volume 41, Issue 8, August 2017, Pages: 1471–1483, Michael Suttie, Leah Wetherill, Sandra W. Jacobson, Joseph L. Jacobson, H. Eugene Hoyme, Elizabeth R. Sowell, Claire Coles, Jeffrey R. Wozniak, Edward P. Riley, Kenneth L. Jones, Tatiana Foroud, Peter Hammond and the CIFASD

    Version of Record online : 10 JUL 2017, DOI: 10.1111/acer.13429

  5. Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation—clinical report and review

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 6, 15 March 2006, Pages: 611–617, Winnie Courtens, Wim Wuyts, Martin Poot, Karoly Szuhai, Jan Wauters, Edwin Reyniers, Marc Eleveld, George Diaz, Markus M. Nöthen and Ruti Parvari

    Version of Record online : 6 FEB 2006, DOI: 10.1002/ajmg.a.31122

  6. Further delineation of the phenotype associated with heterozygous mutations in ZFHX1B

    American Journal of Medical Genetics Part A

    Volume 119A, Issue 3, 15 June 2003, Pages: 257–265, Meredith Wilson, David Mowat, Florence Dastot-Le Moal, Valère Cacheux, Helena Kääriäinen, Danny Cass, Dian Donnai, Jill Clayton-Smith, Sharron Townshend, Cynthia Curry, Michael Gattas, Stephen Braddock, Bronwyn Kerr, Salim Aftimos, Harry Zehnwirth, Catherine Barrey and Michel Goossens

    Version of Record online : 18 MAR 2003, DOI: 10.1002/ajmg.a.20053

  7. New case of interstitial deletion 12(q15-q21.2) in a girl with facial dysmorphism and mental retardation

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 1, 1 January 2008, Pages: 93–96, Caroline Schluth, Roselyne Gesny, Guntram Borck, Richard Redon, Véronique Abadie, Pascale Kleinfinger, Arnold Munnich, Stanislas Lyonnet and Laurence Colleaux

    Version of Record online : 11 DEC 2007, DOI: 10.1002/ajmg.a.31869

  8. Clinical overlap of OFD type IX with Pallister–Killian syndrome (tetrasomy 12p)

    American Journal of Medical Genetics Part A

    Volume 122A, Issue 2, 1 October 2003, Pages: 180–182, D. Geneviève, Y. Sznajer, M. Raoul, D. Sanlaville, A. Verloes, M.F. Portnoï and C. Bauman

    Version of Record online : 3 JUN 2003, DOI: 10.1002/ajmg.a.20306

  9. Duplication Xp11.22-p14 in females: Does X-inactivation help in assessing their significance?

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 553–562, Christina Evers, Diana Mitter, Gertrud Strobl-Wildemann, Ulrich Haug, Karl Hackmann, Bianca Maas, Johannes W. G. Janssen, Anna Jauch, Katrin Hinderhofer and Ute Moog

    Version of Record online : 18 FEB 2015, DOI: 10.1002/ajmg.a.36897

  10. Characterization of six marker chromosomes by comparative genomic hybridization

    American Journal of Medical Genetics Part A

    Volume 136A, Issue 2, 15 July 2005, Pages: 169–174, J.M. Belloso, M.R. Caballín, E. Gabau, N. Baena, R. Vidal, S. Villatoro and M. Guitart

    Version of Record online : 9 JUN 2005, DOI: 10.1002/ajmg.a.30788

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    Facial features in Alagille syndrome: Specific or cholestasis facies?

    American Journal of Medical Genetics

    Volume 112, Issue 2, 1 October 2002, Pages: 163–170, Binita M. Kamath, Kathleen M. Loomes, Rebecca J. Oakey, Karan E.M. Emerick, Tracy Conversano, Nancy B. Spinner, David A. Piccoli and Ian D. Krantz

    Version of Record online : 8 JUL 2002, DOI: 10.1002/ajmg.10579

  12. Diagnostic utility of array-based comparative genomic hybridization in a clinical setting

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 21, 1 November 2007, Pages: 2523–2533, Hagit N. Baris, Wen-Hann Tan, Virginia E. Kimonis and Mira B. Irons

    Version of Record online : 1 OCT 2007, DOI: 10.1002/ajmg.a.31988

  13. A broad spectrum of developmental delay in a large cohort of prolidase deficiency patients demonstrates marked interfamilial and intrafamilial phenotypic variability

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 1, January 2010, Pages: 46–56, Tzipora C. Falik-Zaccai, Morad Khayat, Anthony Luder, Pnina Frenkel, Daniella Magen, Riva Brik, Ruth Gershoni-Baruch and Hanna Mandel

    Version of Record online : 23 MAR 2009, DOI: 10.1002/ajmg.b.30945

  14. Alagille syndrome in a Vietnamese cohort: Mutation analysis and assessment of facial features

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 5, May 2012, Pages: 1005–1013, Henry C. Lin, Phuc Le Hoang, Anne Hutchinson, Grace Chao, Jennifer Gerfen, Kathleen M. Loomes, Ian Krantz, Binita M. Kamath and Nancy B. Spinner

    Version of Record online : 9 APR 2012, DOI: 10.1002/ajmg.a.35255

  15. Genotype–phenotype correlation in eight new patients with a deletion encompassing 2q31.1

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Pages: 1213–1224, Diana Mitter, Barbara Delle Chiaie, Hermann-Josef Lüdecke, Gabriele Gillessen-Kaesbach, Axel Bohring, Jürgen Kohlhase, Almuth Caliebe, Reiner Siebert, Albrecht Roepke, Maria A. Ramos-Arroyo, Beatriz Nieva, Björn Menten, Bart Loeys, Geert Mortier and Dagmar Wieczorek

    Version of Record online : 13 APR 2010, DOI: 10.1002/ajmg.a.33344

  16. The face signature of fibrodysplasia ossificans progressiva

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 6, June 2012, Pages: 1368–1380, Peter Hammond, Michael Suttie, Raoul C. Hennekam, Judith Allanson, Eileen M. Shore and Frederick S. Kaplan

    Version of Record online : 11 MAY 2012, DOI: 10.1002/ajmg.a.35346

  17. Marinesco–Sjögren syndrome in a male with mild dysmorphism

    American Journal of Medical Genetics Part A

    Volume 133A, Issue 2, 1 March 2005, Pages: 197–201, Anne Slavotinek, Jill Goldman, Kara Weisiger, Dana Kostiner, Mahin Golabi, Seymour Packman, William Wilcox, H. Eugene Hoyme and Elliott Sherr

    Version of Record online : 4 JAN 2005, DOI: 10.1002/ajmg.a.30504

  18. 8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients

    American Journal of Medical Genetics Part A

    Volume 161, Issue 3, March 2013, Pages: 487–500, John C.K. Barber, Jill A. Rosenfeld, Nicola Foulds, Sophie Laird, Mark S. Bateman, N. Simon Thomas, Samantha Baker, Viv K. Maloney, Arayamparambil Anilkumar, Wendy E. Smith, Valerie Banks, Sara Ellingwood, Yara Kharbutli, Lakshmi Mehta, Keith A. Eddleman, Michael Marble, Regina Zambrano, John A. Crolla and Allen N. Lamb

    Version of Record online : 23 JAN 2013, DOI: 10.1002/ajmg.a.35767

  19. De novo 11q13.4q14.3 tetrasomy with uniparental isodisomy for 11q14.3qter

    American Journal of Medical Genetics Part A

    Volume 167, Issue 10, October 2015, Pages: 2327–2333, Bing Xiao, Huihui Xu, Hui Ye, Qin Hu, Yingwei Chen and Wenjuan Qiu

    Version of Record online : 10 JUN 2015, DOI: 10.1002/ajmg.a.37179

  20. 36th Annual David W. Smith Workshop on Malformations and Morphogenesis: Abstracts of the 2015 annual meeting

    American Journal of Medical Genetics Part A

    Volume 170, Issue 7, July 2016, Pages: 1665–1726, Karen W. Gripp, Margaret P. Adam, Louanne Hudgins and John C. Carey

    Version of Record online : 27 APR 2016, DOI: 10.1002/ajmg.a.37600