A case report of two male siblings with autism and duplication of Xq13–q21, a region including three genes predisposing for autism-Reference-Cited by-同舟云学术

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A case report of two male siblings with autism and duplication of Xq13–q21, a region including three genes predisposing for autism

Published:2013-08-23 Issue:5 Volume:23 Page:329-336
ISSN:1018-8827
Container-title:European Child & Adolescent Psychiatry
language:en
Short-container-title:Eur Child Adolesc Psychiatry

Author:

Wentz Elisabet,Vujic Mihailo,Kärrstedt Ewa-Lotta,Erlandsson Anna,Gillberg Christopher

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Developmental and Educational Psychology,General Medicine,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00787-013-0455-1.pdf

Reference25 articles.

1. Steinbach P, Horstmann W, Scholz W (1980) Tandem duplication dup(X)(q13q22) in a male proband inherited from the mother showing mosaicism of X-inactivation. Hum Genet 54:309–313

2. Vejerslev LO, Rix M, Jespersen B (1985) Inherited tandem duplication dup(X) (q131–q212) in a male proband. Clin Genet 27:276–281

3. Thode A, Partington MW, Yip MY, Chapman C, Richardson VF et al (1988) A new syndrome with mental retardation, short stature and an Xq duplication. Am J Med Genet 30:239–250

4. Yokoyama Y, Narahara K, Tsuji K, Moriwake T, Kanzaki S et al (1992) Growth hormone deficiency and empty sella syndrome in a boy with dup(X) (q13.3–q21.2). Am J Med Genet 42:660–664

5. Apacik C, Cohen M, Jakobeit M, Schmucker B, Schuffenhauer S et al (1996) Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12–>q13.3) inherited from the mother. Clin Genet 50:63–73

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