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There are 13873 results for: content related to: Growth charts for 22q11 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. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome

    Developmental Disabilities Research Reviews

    Volume 14, Issue 1, 2008, Pages: 26–34, Sarah E. Prasad, Sarah Howley and Kieran C. Murphy

    Version of Record online : 24 MAR 2008, DOI: 10.1002/ddrr.5

  3. Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome

    Journal of Intellectual Disability Research

    Volume 56, Issue 6, June 2012, Pages: 641–651, G. Costain, E. W. C. Chow, P. N. Ray and A. S. Bassett

    Version of Record online : 6 DEC 2011, DOI: 10.1111/j.1365-2788.2011.01510.x

  4. 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

  5. The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population-based study

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 3, March 2012, Pages: 498–508, Peter Agergaard, Charlotte Olesen, John Rosendahl Østergaard, Michael Christiansen and Karina Meden Sørensen

    Version of Record online : 21 DEC 2011, DOI: 10.1002/ajmg.a.34250

  6. 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

  7. Prenatal diagnosis of 22q11.2 deletion syndrome in twin pregnancy: A case report

    Journal of Clinical Ultrasound

    Volume 41, Issue S1, November/December 2013, Pages: 6–9, Ahmet Gul, Kemal Gungorduk, Isil Turan, Gokhan Yildirim, Ali Gedikbasi and Aykut Özdemir

    Version of Record online : 20 SEP 2012, DOI: 10.1002/jcu.21992

  8. Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 24, 15 December 2007, Pages: 2924–2930, Andrea C. Stachon, Berivan Baskin, Adam C. Smith, Andrea Shugar, Cheryl Cytrynbaum, Leona Fishman, Roberto Mendoza-Londono, Regan Klatt, Ahmed Teebi, Peter N. Ray and Rosanna Weksberg

    Version of Record online : 14 NOV 2007, DOI: 10.1002/ajmg.a.32101

  9. Sclerocornea associated with the chromosome 22q11.2 deletion syndrome

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 7, 1 April 2008, Pages: 904–909, Gil Binenbaum, Donna M. McDonald-McGinn, Elaine H. Zackai, B. Michael Walker, Karlene Coleman, Amy M. Mach, Margaret Adam, Melanie Manning, Deborah M. Alcorn, Carrie Zabel, Dennis R. Anderson and Brian J. Forbes

    Version of Record online : 6 MAR 2008, DOI: 10.1002/ajmg.a.32156

  10. Language skills in 5–8-year-old children with 22q11 deletion syndrome

    International Journal of Language & Communication Disorders

    Volume 41, Issue 3, May-June 2006, Pages: 313–333, Christina Persson, Lena Niklasson, Sólveig Óskarsdóttir, Susanne Johansson, Radi Jönsson and Ewa Söderpalm

    Version of Record online : 31 DEC 2010, DOI: 10.1080/13682820500361497

  11. Prevalence of duplications and deletions of the 22q11 DiGeorge syndrome region in a population-based sample of infants with cleft palate

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 2, 15 January 2007, Pages: 129–134, Åse Sivertsen, Rolv Terje Lie, Allen J. Wilcox, Frank Åbyholm, Hallvard Vindenes, Bjørn Ivar Haukanes and Gunnar Houge

    Version of Record online : 12 DEC 2006, DOI: 10.1002/ajmg.a.31445

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    The benefits and limitations of cell-free DNA screening for 22q11.2 deletion syndrome

    Prenatal Diagnosis

    Volume 37, Issue 1, January 2017, Pages: 53–60, Lorraine Dugoff, Michael T. Mennuti and Donna M. McDonald-McGinn

    Version of Record online : 25 JUL 2016, DOI: 10.1002/pd.4864

  13. Developmental perspectives on copy number abnormalities of the 22q11.2 region

    Clinical Genetics

    Volume 78, Issue 3, September 2010, Pages: 201–218, TY Tan, CT Gordon, DJ Amor and PG Farlie

    Version of Record online : 23 APR 2010, DOI: 10.1111/j.1399-0004.2010.01456.x

  14. Increased prevalence of unprovoked seizures in patients with a 22q11.2 deletion

    American Journal of Medical Genetics Part A

    Volume 129A, Issue 1, 15 August 2004, Pages: 29–34, Amy Kao, Juliana Mariani, Donna M. McDonald-McGinn, Melissa K. Maisenbacher, Amy R. Brooks-Kayal, Elaine H. Zackai and David R. Lynch

    Version of Record online : 7 JUN 2004, DOI: 10.1002/ajmg.a.30133

  15. Social cognition dysfunction in adolescents with 22q11.2 deletion syndrome (velo-cardio-facial syndrome): relationship with executive functioning and social competence/functioning

    Journal of Intellectual Disability Research

    Volume 59, Issue 9, September 2015, Pages: 845–859, L. E. Campbell, K. L. McCabe, J. L. Melville, P. A. Strutt and U. Schall

    Version of Record online : 25 FEB 2015, DOI: 10.1111/jir.12183

  16. Intellectual functioning in relation to autism and ADHD symptomatology in children and adolescents with 22q11.2 deletion syndrome

    Journal of Intellectual Disability Research

    Volume 59, Issue 9, September 2015, Pages: 803–815, E. Hidding, H. Swaab, L. M. J. de Sonneville, H. van Engeland, M. E. J. Sijmens-Morcus, P. W. J. Klaassen, S. N. Duijff and J. A. S. Vorstman

    Version of Record online : 13 FEB 2015, DOI: 10.1111/jir.12187

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    Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 1, 5 January 2007, Pages: 27–36, Kathryn Eve Lewandowski, Vandana Shashi, Peggy M. Berry and Thomas R. Kwapil

    Version of Record online : 10 OCT 2006, DOI: 10.1002/ajmg.b.30379

  18. Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 9, 1 May 2008, Pages: 1134–1141, Luis Fernández, Pablo Lapunzina, Isidora López Pajares, María Palomares, Isabel Martínez, Blanca Fernández, José Quero, Luis García-Guereta, Alfredo García-Alix, Margarita Burgueros, Enrique Galán-Gómez, José María Carbonell-Pérez, Ángeles Pérez-Granero, Laura Torres-Juan, Damià Heine-Suñer, Jordi Rosell and Alicia Delicado

    Version of Record online : 2 APR 2008, DOI: 10.1002/ajmg.a.32256

  19. Antibody deficiency in adults with 22q11.2 deletion syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 8, August 2012, Pages: 1934–1940, Aron H. Björk, Sólveig Óskarsdóttir, Bengt A. Andersson and Vanda Friman

    Version of Record online : 11 JUL 2012, DOI: 10.1002/ajmg.a.35484

  20. You have free access to this content
    Syndrome-specific growth charts for 22q11.2 deletion syndrome in Caucasian children

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2665–2671, Alex Habel, Michael-John McGinn II, Elaine H. Zackai, Nancy Unanue and Donna M. McDonald-McGinn

    Version of Record online : 18 JUN 2012, DOI: 10.1002/ajmg.a.35426