Autism in children with 22Q11.2 deletion syndrome - Reply

被引：1
|
作者：
Vorstman, Jacob A. S. [1 ]
Morcus, Monique E. J. [1 ]
van Engeland, Herman [1 ]
机构：
[1] Univ Utrecht, Med Ctr, Rudolf Magnus Inst Neurosci, Utrecht, Netherlands
来源：
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY | 2007年 / 46卷 / 04期
关键词：
D O I：
10.1097/chi.0b013e3180303b7d
中图分类号：
B844 [发展心理学（人类心理学）];
学科分类号：
040202 ;
摘要：
引用
收藏
页码：434 / 435
页数：2
相关论文
共 50 条
  • [41] Developmental trajectories in 22q11.2 deletion syndrome
    Swillen, Ann
    McDonald-McGinn, Donna
    AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2015, 169 (02) : 172 - 181
  • [42] Olfactory deficits in deletion syndrome 22q11.2
    Romanos, Marcel
    Schecklmann, Martin
    Kraus, Katharina
    Fallgatter, Andreas J.
    Warnke, Andreas
    Lesch, Klaus-Peter
    Gerlach, Manfred
    SCHIZOPHRENIA RESEARCH, 2011, 129 (2-3) : 220 - 221
  • [43] Labyrinthine malformation in the 22q11.2 deletion syndrome
    Hopsu, Erkki
    Markkola, Antti
    Pitkaranta, Anne
    CLINICAL DYSMORPHOLOGY, 2007, 16 (01) : 67 - 68
  • [44] 22q11.2 deletion syndrome in diverse populations
    Kruszka, Paul
    Addissie, Yonit A.
    McGinn, Daniel E.
    Porras, Antonio R.
    Biggs, Elijah
    Share, Matthew
    Crowley, T. Blaine
    Chung, Brian H. Y.
    Mok, Gary T. K.
    Mak, Christopher C. Y.
    Muthukumarasamy, Premala
    Thong, Meow-Keong
    Sirisena, Nirmala D.
    Dissanayake, Vajira H. W.
    Paththinige, C. Sampath
    Prabodha, L. B. Lahiru
    Mishra, Rupesh
    Shotelersuk, Vorasuk
    Ekure, Ekanem Nsikak
    Sokunbi, Ogochukwu Jidechukwu
    Kalu, Nnenna
    Ferreira, Carlos R.
    Duncan, Jordann-Mishael
    Patil, Siddaramappa Jagdish
    Jones, Kelly L.
    Kaplan, Julie D.
    Abdul-Rahman, Omar A.
    Uwineza, Annette
    Mutesa, Leon
    Moresco, Angelica
    Gabriela Obregon, Maria
    Richieri-Costa, Antonio
    Gil-da-Silva-Lopes, Vera L.
    Adeyemo, Adebowale A.
    Summar, Marshall
    Zackai, Elaine H.
    McDonald-McGinn, Donna M.
    Linguraru, Marius George
    Muenke, Maximilian
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (04) : 879 - 888
  • [45] Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndrome
    Lima, Kari
    Abrahamsen, Tore G.
    Wolff, Anette Boe
    Husebye, Eystein
    Alimohammadi, Mohammad
    Kampe, Olle
    Folling, Ivar
    EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2011, 165 (02) : 345 - 352
  • [46] Immunodeficiency and autoimmunity in 22q11.2 deletion syndrome
    McLean-Tooke, A.
    Spickett, G. P.
    Gennery, A. R.
    SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2007, 66 (01) : 1 - 7
  • [47] Opitz GBBB syndrome and the 22q11.2 deletion
    Lacassie, Y
    Arriaza, MI
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1996, 62 (03): : 318 - 318
  • [48] Complement Activation in 22q11.2 Deletion Syndrome
    Dina Grinde
    Torstein Øverland
    Kari Lima
    Camilla Schjalm
    Tom Eirik Mollnes
    Tore G. Abrahamsen
    Journal of Clinical Immunology, 2020, 40 : 515 - 523
  • [49] Neuroradiographic findings in 22q11.2 deletion syndrome
    Bohm, Lauren A.
    Zhou, Tom C.
    Mingo, Tyler J.
    Dugan, Sarah L.
    Patterson, Richard J.
    Sidman, James D.
    Roby, Brianne B.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (08) : 2158 - 2165
  • [50] Heterotopia in Individuals with 22q11.2 Deletion Syndrome
    Neuhaus, E.
    Hattingen, E.
    Breuer, S.
    Steidl, E.
    Polomac, N.
    Rosenow, F.
    Rueber, T.
    Herrmann, E.
    Ecker, C.
    Kushan, L.
    Lin, A.
    Vajdi, A.
    Bearden, C. E.
    Jurcoane, A.
    AMERICAN JOURNAL OF NEURORADIOLOGY, 2021, 42 (11) : 2070 - 2076
12345