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There are 2551 results for: content related to: Disorders of left ventricular trabeculation/compaction or right ventricular wall formation

  1. Angelman syndrome in adulthood

    American Journal of Medical Genetics Part A

    Volume 167, Issue 2, February 2015, Pages: 331–344, Anna M. Larson, Julianna E. Shinnick, Elias A. Shaaya, Elizabeth A. Thiele and Ronald L. Thibert

    Article first published online : 26 NOV 2014, DOI: 10.1002/ajmg.a.36864

  2. Epidemiology of fragile X syndrome: A systematic review and meta-analysis

    American Journal of Medical Genetics Part A

    Volume 164, Issue 7, July 2014, Pages: 1648–1658, Jessica Hunter, Oliver Rivero-Arias, Angel Angelov, Edward Kim, Iain Fotheringham and Jose Leal

    Article first published online : 3 APR 2014, DOI: 10.1002/ajmg.a.36511

  3. You have free access to this content
    Association of genetic risk severity with ADHD clinical characteristics

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 7, October 2013, Pages: 718–733, Amelia Kotte, Stephen V. Faraone and Joseph Biederman

    Article first published online : 17 OCT 2013, DOI: 10.1002/ajmg.b.32171

  4. 9p partial monosomy and disorders of sex development: Review and postulation of a pathogenetic mechanism

    American Journal of Medical Genetics Part A

    Volume 161, Issue 8, August 2013, Pages: 1882–1896, Shane C. Quinonez, John M. Park, Raja Rabah, Kailey M. Owens, Beverly M. Yashar, Thomas W. Glover and Catherine E. Keegan

    Article first published online : 3 JUL 2013, DOI: 10.1002/ajmg.a.36018

  5. Modeling anterior development in mice: Diet as modulator of risk for neural tube defects

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 163, Issue 4, November 2013, Pages: 333–356, Claudia Kappen

    Article first published online : 4 OCT 2013, DOI: 10.1002/ajmg.c.31380

  6. Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 1, January 2014, Pages: 41–51, Claudine M. Kraan, Darren R. Hocking, Nellie Georgiou-Karistianis, Sylvia A. Metcalfe, Alison D. Archibald, Joanne Fielding, Julian Trollor, John L. Bradshaw, Jonathan Cohen and Kim M. Cornish

    Article first published online : 26 OCT 2013, DOI: 10.1002/ajmg.b.32203

  7. You have full text access to this OnlineOpen article
    Language and traits of autism spectrum conditions: Evidence of limited phenotypic and etiological overlap

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 7, October 2014, Pages: 587–595, Mark J. Taylor, Tony Charman, Elise B. Robinson, Marianna E. Hayiou-Thomas, Francesca Happé, Philip S. Dale and Angelica Ronald

    Article first published online : 2 AUG 2014, DOI: 10.1002/ajmg.b.32262

  8. Anxiety, attention problems, hyperactivity, and the Aberrant Behavior Checklist in fragile X syndrome

    American Journal of Medical Genetics Part A

    Volume 164, Issue 1, January 2014, Pages: 141–155, Anne Wheeler, Melissa Raspa, Carla Bann, Ellen Bishop, David Hessl, Pat Sacco and Donald B. Bailey Jr.

    Article first published online : 25 NOV 2013, DOI: 10.1002/ajmg.a.36232

  9. Megalencephaly and hemimegalencephaly: Breakthroughs in molecular etiology

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 166, Issue 2, June 2014, Pages: 156–172, Ghayda M. Mirzaa and Annapurna Poduri

    Article first published online : 28 MAY 2014, DOI: 10.1002/ajmg.c.31401

  10. Synergistic association of PI4KA and GRM3 genetic polymorphisms with poor antipsychotic response in south Indian schizophrenia patients with low severity of illness

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 8, December 2014, Pages: 635–646, Harpreet Kaur, Ajay Jajodia, Sandeep Grover, Ruchi Baghel, Sanjeev Jain and Ritushree Kukreti

    Article first published online : 10 SEP 2014, DOI: 10.1002/ajmg.b.32268

  11. You have free access to this content
    Amyoplasia revisited

    American Journal of Medical Genetics Part A

    Volume 164, Issue 3, March 2014, Pages: 700–730, Judith G. Hall, Kimberly A. Aldinger and Kimi I. Tanaka

    Article first published online : 23 JAN 2014, DOI: 10.1002/ajmg.a.36395

  12. Understanding the basis of auriculocondylar syndrome: Insights from human, mouse and zebrafish genetic studies

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 163, Issue 4, November 2013, Pages: 306–317, David E. Clouthier, Maria Rita Passos-Bueno, Andre L.P. Tavares, Stanislas Lyonnet, Jeanne Amiel and Christopher T. Gordon

    Article first published online : 4 OCT 2013, DOI: 10.1002/ajmg.c.31376

  13. You have full text access to this OnlineOpen article
    Evaluating the role of a galanin enhancer genotype on a range of metabolic, depressive and addictive phenotypes

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 8, December 2014, Pages: 654–664, Tom G. Richardson, Camelia Minica, Jon Heron, Jeremy Tavare, Alasdair MacKenzie, Ian Day, Glyn Lewis, Matthew Hickman, Jacqueline M. Vink, Joel Gelernter, Henry R. Kranzler, Lindsay A Farrer, Marcus Munafò and David Wynick

    Article first published online : 16 SEP 2014, DOI: 10.1002/ajmg.b.32270

  14. Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesity

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 4, June 2014, Pages: 283–293, Anke Hinney, Özgür Albayrak, Jochen Antel, Anna-Lena Volckmar, Rebecca Sims, Jade Chapman, Denise Harold, Amy Gerrish, Iris M. Heid, Thomas W. Winkler, André Scherag, Jens Wiltfang, Julie Williams, Johannes Hebebrand, GERAD Consortium, IGAP Consortium and GIANT Consortium

    Article first published online : 1 MAY 2014, DOI: 10.1002/ajmg.b.32234

  15. Amyoplasia involving only the upper limbs or only involving the lower limbs with review of the relevant differential diagnoses

    American Journal of Medical Genetics Part A

    Volume 164, Issue 4, April 2014, Pages: 859–873, Judith G. Hall

    Article first published online : 23 JAN 2014, DOI: 10.1002/ajmg.a.36397

  16. The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 166, Issue 3, September 2014, Pages: 315–326, Geert Vandeweyer, Céline Helsmoortel, Anke Van Dijck, Anneke T. Vulto-van Silfhout, Bradley P. Coe, Raphael Bernier, Jennifer Gerdts, Liesbeth Rooms, Jenneke van den Ende, Madhura Bakshi, Meredith Wilson, Ann Nordgren, Laura G. Hendon, Omar A. Abdulrahman, Corrado Romano, Bert B.A. de Vries, Tjitske Kleefstra, Evan E. Eichler, Nathalie Van der Aa and R. Frank Kooy

    Article first published online : 28 AUG 2014, DOI: 10.1002/ajmg.c.31413

  17. Association of microcephalin 1, syntrophin-beta 1, and other genes with automatic thoughts in the Japanese population

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 6, September 2014, Pages: 492–501, Yoshinobu Ishitobi, Ayako Inoue, Saeko Aizawa, Koji Masuda, Tomoko Ando, Aimi Kawano, Rie Ikeda, Yoshihiro Maruyama, Masayuki Kanehisa, Taiga Ninomiya, Yoshihiro Tanaka, Jusen Tsuru and Jotaro Akiyoshi

    Article first published online : 29 JUN 2014, DOI: 10.1002/ajmg.b.32252

  18. Genotype and clinical care correlations in craniosynostosis: Findings from a cohort of 630 Australian and New Zealand patients

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 163, Issue 4, November 2013, Pages: 259–270, T. Roscioli, G. Elakis, T.C. Cox, D.J. Moon, H. Venselaar, A.M. Turner, T. Le, E. Hackett, E. Haan, A. Colley, D. Mowat, L. Worgan, E.P. Kirk, R. Sachdev, E. Thompson, M. Gabbett, J. McGaughran, K. Gibson, M. Gattas, M-L. Freckmann, J. Dixon, L. Hoefsloot, M. Field, A. Hackett, B. Kamien, M. Edwards, L.C. Adès, F.A. Collins, M.J. Wilson, R. Savarirayan, T.Y. Tan, D.J. Amor, G. McGIllivray, S.M. White, I.A. Glass, D.J. David, P.J. Anderson, M. Gianoutsos and M.F. Buckley

    Article first published online : 11 OCT 2013, DOI: 10.1002/ajmg.c.31378

  19. Targeted methylation testing of a patient cohort broadens the epigenetic and clinical description of imprinting disorders

    American Journal of Medical Genetics Part A

    Volume 161, Issue 9, September 2013, Pages: 2174–2182, Rebecca L. Poole, Louise E. Docherty, Abeer Al Sayegh, Almuth Caliebe, Claire Turner, Emma Baple, Emma Wakeling, Lucy Harrison, Anna Lehmann, I. Karen Temple, Deborah J.G. Mackay and On behalf of the International Clinical Imprinting Consortium

    Article first published online : 2 AUG 2013, DOI: 10.1002/ajmg.a.36049

  20. Perinatal features of the RASopathies: Noonan syndrome, Cardiofaciocutaneous syndrome and Costello syndrome

    American Journal of Medical Genetics Part A

    Volume 164, Issue 11, November 2014, Pages: 2814–2821, Angela Myers, Jonathan A. Bernstein, Marie-Luise Brennan, Cynthia Curry, Edward D. Esplin, Jamie Fisher, Margaret Homeyer, Melanie A. Manning, Eric A. Muller, Anna-Kaisa Niemi, Laurie H. Seaver, Susan R. Hintz and Louanne Hudgins

    Article first published online : 22 SEP 2014, DOI: 10.1002/ajmg.a.36737