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There are 10897 results for: content related to: Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome

  1. Developmental trajectories in 22q11.2 deletion syndrome

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

    Volume 169, Issue 2, June 2015, Pages: 172–181, Ann Swillen and Donna McDonald-McGinn

    Version of Record online : 18 MAY 2015, DOI: 10.1002/ajmg.c.31435

  2. Congenital diaphragmatic hernia in 22q11.2 deletion syndrome

    American Journal of Medical Genetics Part A

    Marta Unolt, Lauren DiCairano, Kathryn Schlechtweg, Jessica Barry, Lori Howell, Stefanie Kasperski, Michael Nance, N. Scott Adzick, Elaine H. Zackai and Donna M. McDonald-McGinn

    Version of Record online : 28 SEP 2016, DOI: 10.1002/ajmg.a.37980

  3. Currently recognized genes for schizophrenia: High-resolution chromosome ideogram representation

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 2, March 2016, Pages: 181–202, Merlin G. Butler, Austen B. McGuire, Humaira Masoud and Ann M. Manzardo

    Version of Record online : 13 OCT 2015, DOI: 10.1002/ajmg.b.32391

  4. You have full text access to this OnlineOpen article
    Craniofacial dysmorphology in 22q11.2 deletion syndrome by 3D laser surface imaging and geometric morphometrics: Illuminating the developmental relationship to risk for psychosis

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 529–536, Sarah Prasad, Stanislav Katina, Robin J. Hennessy, Kieran C. Murphy, Adrian W. Bowman and John L. Waddington

    Version of Record online : 18 FEB 2015, DOI: 10.1002/ajmg.a.36893

  5. You have free access to this content
    Disorders and borders: Psychiatric genetics and nosology

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 7, October 2013, Pages: 559–578, Jordan W. Smoller

    Version of Record online : 17 OCT 2013, DOI: 10.1002/ajmg.b.32174

  6. IQ and hemizygosity for the Val158Met functional polymorphism of COMT in 22q11DS

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 8, December 2016, Pages: 1112–1115, Colleen P. Franconi, Donna McDonald-McGinn, Elaine H. Zackai, Meghan A. McNamara, Harold Salmons IV, Edward Moss, Raquel E. Gur, Marcella Devoto and Beverly S. Emanuel

    Version of Record online : 13 SEP 2016, DOI: 10.1002/ajmg.b.32492

  7. Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 639–645, Erik Boot, Nancy J Butcher, Thérèse AMJ van Amelsvoort, Anthony E Lang, Connie Marras, Margarita Pondal, Danielle M Andrade, Wai Lun Alan Fung and Anne S Bassett

    Version of Record online : 13 FEB 2015, DOI: 10.1002/ajmg.a.36928

  8. Central 22q11.2 deletions

    American Journal of Medical Genetics Part A

    Volume 164, Issue 11, November 2014, Pages: 2707–2723, Patrick Rump, Nicole de Leeuw, Anthonie J. van Essen, Corien C. Verschuuren-Bemelmans, Hermine E. Veenstra-Knol, Mariëlle E.M. Swinkels, Wilma Oostdijk, Claudia Ruivenkamp, Willie Reardon, Sonja de Munnik, Mariken Ruiter, Ayala Frumkin, Dorit Lev, Christina Evers, Birgit Sikkema-Raddatz, Trijnie Dijkhuizen and Conny M. van Ravenswaaij-Arts

    Version of Record online : 14 AUG 2014, DOI: 10.1002/ajmg.a.36711

  9. 5p deletions: Current knowledge and future directions

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

    Volume 169, Issue 3, September 2015, Pages: 224–238, Joanne M. Nguyen, Krista J. Qualmann, Rebecca Okashah, AmySue Reilly, Mikhail F. Alexeyev and Dennis J. Campbell

    Version of Record online : 3 AUG 2015, DOI: 10.1002/ajmg.c.31444

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    The neurobiological basis of human aggression: A review on genetic and epigenetic mechanisms

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 5, July 2016, Pages: 650–675, Regina Waltes, Andreas G. Chiocchetti and Christine M. Freitag

    Version of Record online : 22 OCT 2015, DOI: 10.1002/ajmg.b.32388

  11. Autism and epistemology IV: Does autism need a theory of mind?

    American Journal of Medical Genetics Part A

    Volume 161, Issue 10, October 2013, Pages: 2464–2480, Gene S. Fisch

    Version of Record online : 16 AUG 2013, DOI: 10.1002/ajmg.a.36135

  12. Review of X-linked syndromes with arthrogryposis or early contractures—aid to diagnosis and pathway identification

    American Journal of Medical Genetics Part A

    Volume 167, Issue 5, May 2015, Pages: 931–973, Jesse M. Hunter, Jeff Kiefer, Christopher D. Balak, Sonya Jooma, Mary Ellen Ahearn, Judith G. Hall and Lisa Baumbach-Reardon

    Version of Record online : 19 MAR 2015, DOI: 10.1002/ajmg.a.36934

  13. An increased prevalence of thyroid disease in children with 22q11.2 deletion syndrome

    American Journal of Medical Genetics Part A

    Volume 167, Issue 7, July 2015, Pages: 1560–1564, Andrea L. Shugar, Jessica M. Shapiro, Cheryl Cytrynbaum, Stephanie Hedges, Rosanna Weksberg and Leona Fishman

    Version of Record online : 5 MAY 2015, DOI: 10.1002/ajmg.a.37064

  14. Genetic counseling and testing for Huntington's disease: A historical review

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Martha A. Nance

    Version of Record online : 13 MAY 2016, DOI: 10.1002/ajmg.b.32453

  15. SWI/SNF chromatin remodeling complexes and cancer

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

    Volume 166, Issue 3, September 2014, Pages: 350–366, Jaclyn A. Biegel, Tracy M. Busse and Bernard E. Weissman

    Version of Record online : 28 AUG 2014, DOI: 10.1002/ajmg.c.31410

  16. 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

    Version of Record online : 4 OCT 2013, DOI: 10.1002/ajmg.c.31380

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    Social cognition as an RDoC domain

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 1, January 2016, Pages: 132–141, Ruben C. Gur and Raquel E. Gur

    Version of Record online : 26 NOV 2015, DOI: 10.1002/ajmg.b.32394

  18. Etiologies of uterine malformations

    American Journal of Medical Genetics Part A

    Volume 170, Issue 8, August 2016, Pages: 2141–2172, Adeline Jacquinet, Debra Millar and Anna Lehman

    Version of Record online : 8 JUN 2016, DOI: 10.1002/ajmg.a.37775

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    A review of neuroimaging studies of young relatives of individuals with schizophrenia: A developmental perspective from schizotaxia to schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 7, October 2013, Pages: 604–635, H.W. Thermenos, M.S. Keshavan, R.J. Juelich, E. Molokotos, S. Whitfield-Gabrieli, B.K. Brent, N. Makris and L.J. Seidman

    Version of Record online : 17 OCT 2013, DOI: 10.1002/ajmg.b.32170

  20. You have free access to this content
    Aggression in non-human vertebrates: Genetic mechanisms and molecular pathways

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 5, July 2016, Pages: 603–640, Florian Freudenberg, Hector Carreño Gutierrez, Antonia M. Post, Andreas Reif and William H. J. Norton

    Version of Record online : 18 AUG 2015, DOI: 10.1002/ajmg.b.32358