Abilities and attainment in Smith-Magenis syndrome

Developmental Medicine and Child Neurology

Volumn 43, Issue 12, 2001, Pages 823-828

  Udwin, Orlee ^a,c   Horn, Isobel ^b  

^a Child and Adolescent Mental Health Service   (United Kingdom)

^b SOUTH LONDON AND MAUDSLEY NHS FOUNDATION TRUST   (United Kingdom)

^c Mary Sheridan Centre for Child Health   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADAPTIVE BEHAVIOR; ADOLESCENT; ADULT; ARTICLE; BEHAVIOR DISORDER; BOY; CAREGIVER; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COGNITION; DISEASE SEVERITY; FEMALE; GIRL; HUMAN; INDEPENDENCE; INTELLIGENCE; INTELLIGENCE QUOTIENT; LEARNING DISORDER; MALE; MENTAL CAPACITY; PRIORITY JOURNAL; SCHOOL; SMITH MAGENIS SYNDROME; SOCIOECONOMICS; TASK PERFORMANCE; VERBAL BEHAVIOR;

EID: 0035207224     PISSN: 00121622     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1469-8749.2001.tb00170.x     Document Type: Article

References (23)

1. Ophthalmic manifestations of Smith-Magenis syndrome
2. The Smith-Magenis syndrome del(17) p11.2: Clinical review and molecular advances
3. Clinical and chromosome studies of three patients with Smith-Magenis syndrome
4. Stage transitioning in the sensori-motor development of Down's Syndrome infants
5. Cognitive and behavioural profiles in persons with Smith-Magenis syndrome
6. Distinctiveness and correlates of maladaptive behaviour in children and adolescents with Smith-Magenis syndrome
7. Smith-Magenis syndrome due to a submicroscopic deletion in 17p11.2 allows further definition of the critical interval
8. Eye abnormalities in the Smith-Magenis contiguous gene deletion syndrome
9. The spasmodic upper-body squeeze: A characteristic behavior in Smith-Magenis syndrome
10. Molecular analysis of the Smith-Magenis syndrome: A possible contiguous-gene syndrome associated with del(17)(p11.2)
11. Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)
12. Longitudinal IQ changes in fragile X males
13. Smith-Magenis syndrome: A new contiguous gene syndrome: Report of three new cases
14. Deletion of the 17 short arm in two patients with facial clefts
15. Interstitial deletion of (17) (p11.2p11.2) in nine patients
16. Sleep disturbance in Smith-Magenis syndrome (del 17 p11.2)
17. Case reports of autism with interstitial deletion of chromosome 17 (p11.2p11.2) and monosomy of chromosome 5 (5pter→5p15.3)
18. Clinical, cytogenetic and molecular evidence for an infant with SMS born from a mother having a mosaic 17p11.2p12 deletion