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PMID: 9105971 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Brief report: cognitive and behavioral profiles in persons with Smith-Magenis syndrome.

Journal of autism and developmental disorders ·Vol. 27 ·No. 2 ·1997-04-00 ·Pages 203-11

Dykens EM, Finucane BM, Gayley C

Abstract

暂无摘要

MeSH Terms
Abnormalities, Multiple/genetics,psychology Adolescent Adult Chromosomes, Human, Pair 17 Cognition Female Gene Deletion Humans Intellectual Disability Male Middle Aged Motor Activity Sleep Wake Disorders Social Behavior Disorders Syndrome
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Dykens E M
UCLA Neuropsychiatric Institute, USA.
Finucane B M
Gayley C
References (9)
9 references, click to expand
  1. Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p11.2 p11.2) (Smith-Magenis syndrome).
    J Paediatr Child Health. 1990 Feb;26(1):17-21 PMID: 2331413
  2. Eye abnormalities in the Smith-Magenis contiguous gene deletion syndrome.
    Am J Med Genet. 1993 Feb 15;45(4):443-6 PMID: 8465847
  3. K-ABC profiles in children with fragile X syndrome, Down syndrome, and nonspecific mental retardation.
    Am J Ment Retard. 1992 Jul;97(1):39-46 PMID: 1386742
  4. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
    Am J Med Genet. 1986 Jul;24(3):421-32 PMID: 3728561
  5. The spasmodic upper-body squeeze: a characteristic behavior in Smith-Magenis syndrome.
    Dev Med Child Neurol. 1994 Jan;36(1):78-83 PMID: 8132119
  6. Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).
    Am J Hum Genet. 1991 Dec;49(6):1207-18 PMID: 1746552
  7. Interstitial deletion of (17)(p11.2p11.2) in nine patients.
    Am J Med Genet. 1986 Jul;24(3):393-414 PMID: 2425619
  8. Measuring behavioral phenotypes: provocations from the "new genetics".
    Am J Ment Retard. 1995 Mar;99(5):522-32 PMID: 7779347
  9. Profiles, correlates, and trajectories of intelligence in Prader-Willi syndrome.
    J Am Acad Child Adolesc Psychiatry. 1992 Nov;31(6):1125-30 PMID: 1429416
Article Info
Journal
Journal of autism and developmental disorders
Abbr.
J Autism Dev Disord
ISSN
0162-3257
DOI
10.1023/a:1025800126086
Published
1997-04-00
Pages
203-11
Language
English
Region
United States
NLM ID
7904301
Subset
IM
Grants
PHS HHS · 730Z · United States
External Links
PubMed source DOI: 10.1023/a:1025800126086 View journal details
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