14q32.3 deletion syndrome with autism [1]

American Journal of Medical Genetics

Volumn 133 A, Issue 1, 2005, Pages 99-100

  Babovic Vuksanovic, Dusica ^a   Merritt II, J Lawrence ^a   Jalal, Syed M ^a   Barbaresi, William J ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; BLEPHAROPHIMOSIS; CASE REPORT; CHROMOSOME 14; CHROMOSOME 21; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DISORDER; CHROMOSOME PAINTING; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CLINODACTYLY; COGNITIVE DEFECT; CONVERGENT STRABISMUS; ELECTROENCEPHALOGRAM; EPICANTHUS; FAILURE TO THRIVE; FEEDING DISORDER; FEMALE; FOCAL EPILEPSY; GROWTH RETARDATION; HUMAN; HYPERTELORISM; INGUINAL HERNIA; KARYOTYPING; LETTER; MICROCEPHALY; MUSCLE HYPOTONIA; OTITIS MEDIA; PETIT MAL; PRESCHOOL CHILD; PRIORITY JOURNAL; PTOSIS; SCORING SYSTEM;

AUTISTIC DISORDER; CHILD; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 21; DEVELOPMENTAL DISABILITIES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; SYNDROME; TRANSLOCATION, GENETIC;

EID: 12944272023     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30462     Document Type: Letter

References (2)

1. Diagnostic and Statistical Manual of Mental Disorders Text Revision (DSMTR). 2000. 4th edn. Washington DC: American Psychiatric Association.
2. Ortigas AP, Stein CK, Thomson LL, Hoo JJ. 1997. Delineation of 14q32.3 deletion syndrome. J Med Genet 34:515-517.