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There are 23663 results for: content related to: Syndrome-specific growth charts for 22q11.2 deletion syndrome in Caucasian children

  1. 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

  2. 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

  3. 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

  4. 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

  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. 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

  7. Chromosome 22q11 deletion syndrome: Update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications

    American Journal of Medical Genetics

    Volume 97, Issue 2, Summer 2000, Pages: 128–135, A. Swillen, A. Vogels, K. Devriendt and J. P. Fryns

    Version of Record online : 28 NOV 2000, DOI: 10.1002/1096-8628(200022)97:2<128::AID-AJMG4>3.0.CO;2-Z

  8. Can we predict 22q11 status of fetuses with tetralogy of Fallot?

    Prenatal Diagnosis

    Volume 22, Issue 3, March 2002, Pages: 231–234, Younes Boudjemline, Laurent Fermont, Jérôme Le Bidois, Elizabeth Villain, Daniel Sidi and Damien Bonnet

    Version of Record online : 12 MAR 2002, DOI: 10.1002/pd.295

  9. Variation in prevalence of chromosome 22q11 deletion in subtypes of conotruncal defect in 254 children

    Acta Paediatrica

    Volume 100, Issue 9, September 2011, Pages: e97–e100, A Anilkumar, M Kappanayil, MV Thampi, S Nampoothiri, KR Sundaram and DM Vasudevan

    Version of Record online : 7 APR 2011, DOI: 10.1111/j.1651-2227.2011.02271.x

  10. 22q11 deletion syndrome in adults with schizophrenia

    American Journal of Medical Genetics

    Volume 81, Issue 4, 10 July 1998, Pages: 328–337, Anne S. Bassett, Kathy Hodgkinson, Eva W.C. Chow, Susana Correia, Laura E. Scutt and Rosanna Weksberg

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19980710)81:4<328::AID-AJMG10>3.0.CO;2-N

  11. DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion

    American Journal of Medical Genetics Part A

    Volume 117A, Issue 1, 15 February 2003, Pages: 1–5, Oliver Bartsch, Michaela Nemecková, Eduard Kocárek, Annett Wagner, Alena Puchmajerová, Maja Poppe, Katrin Ounap and Petr Goetz

    Version of Record online : 18 SEP 2002, DOI: 10.1002/ajmg.a.10914

  12. 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

  13. 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

  14. You have free access to this content
    Growth charts for 22q11 deletion syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2672–2681, Daniel C. Tarquinio, Marilyn C. Jones, Kenneth Lyons Jones and Lynne M. Bird

    Version of Record online : 6 AUG 2012, DOI: 10.1002/ajmg.a.35485

  15. Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 22, 15 November 2006, Pages: 2426–2432, Anna Brunet, Elisabeth Gabau, Rosa Maria Perich, Laura Valdesoiro, Carme Brun, Maria Rosa Caballín and Miriam Guitart

    Version of Record online : 13 OCT 2006, DOI: 10.1002/ajmg.a.31499

  16. 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

  17. 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

  18. Detailed analysis of 22q11.2 with a high density MLPA probe set

    Human Mutation

    Volume 29, Issue 3, March 2008, Pages: 433–440, G.R. Jalali, J.A.S. Vorstman, Ab Errami, R. Vijzelaar, J. Biegel, T. Shaikh and B.S. Emanuel

    Version of Record online : 21 NOV 2007, DOI: 10.1002/humu.20640

  19. 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

  20. You have free access to this content
    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