Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p 11.2 p 11.2) (Smith‐Magenis syndrome)

Journal of Paediatrics and Child Health

Volumn 26, Issue 1, 1990, Pages 17-21

  COLLEY, A F ^a   LEVERSHA, M A ^a   VOULLAIRE, L E ^a   ROGERS, J G ^a  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

Abnormal behaviour; chromosome deletion; hyperactivity; self mutilation; sleep disturbance; Smith Magenis syndrome

Indexed keywords

ARTICLE; BEHAVIOR DISORDER; CHROMOSOME 17P; CHROMOSOME DELETION; FEMALE; HUMAN; HYPERACTIVITY; KARYOTYPING; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; PRIORITY JOURNAL; PSYCHOLOGICAL ASPECT; SYMPTOMATOLOGY; SYNDROME DELINEATION;

EID: 0025218940     PISSN: 10344810     EISSN: 14401754     Source Type: Journal    
DOI: 10.1111/j.1440-1754.1990.tb02372.x     Document Type: Article

References (5)

1. Deletion of the 17 short arm in two patients with facial clefts
2. Interstitial deletion of (17))(p 11.2 p 11.2): Report of six additional patients with a new chromosome deletion syndrome
3. Interstitial deletion of (17)(p 11.2 p. 11.2) in nine patients
4. Interstitial deletion of 17 p 11.2: Case report and review
5. Chromosome subband 17p 11.2 deletion: A minute deletion syndrome