Neurodevelopmental and behavioral abnormalities associated with deletion of chromosome 9p

Journal of Child Neurology

Volumn 17, Issue 1, 2002, Pages 50-51

  Eshel, Gideon ^a   Lahat, Eli ^a   Reish, Orit ^a   Barr, Joseph ^a  

^a ASSAF HAROFEH MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BEHAVIOR DISORDER; CASE REPORT; CHROMOSOME 9P; CHROMOSOME DELETION; CLINICAL FEATURE; CORPUS CALLOSUM AGENESIS; CRANIOFACIAL SYNOSTOSIS; DEVELOPMENTAL DISORDER; DIFFERENTIAL DIAGNOSIS; FEMALE; GROWTH RETARDATION; HUMAN; MALE; MALFORMATION SYNDROME; PRECOCIOUS PUBERTY; PRIORITY JOURNAL; SCHOOL CHILD;

ABNORMALITIES, MULTIPLE; BRAIN; CHILD; CHILD BEHAVIOR DISORDERS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 9; CORPUS CALLOSUM; CRANIOSYNOSTOSES; DEVELOPMENTAL DISABILITIES; DISEASES IN TWINS; FEMALE; HUMANS;

EID: 0036122084     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307380201700113     Document Type: Article

References (5)

1. Deletion of the short arm of chromosome 9 (46,9p): A new deletion syndrome
2. Eleven new cases of del (9p) and features from 80 cases
3. Chromosome 9, partial monosomy 9p
4. A case of the novo interstitial deletion of chromosome 9(p12p13)
5. Practice parameters for the assessment and treatment of children, adolescents, and adults with attention-deficit/hyperactivity disorder