Inverted duplication/deletion of chromosome 8p: Mild clinical phenotype [3]

American Journal of Medical Genetics

Volumn 82, Issue 1, 1999, Pages 91-93

  Yenamandra, A ^a   Perrone, R ^a   McLaughlin, J ^a   Mehta, L ^a  

^a NORTH SHORE UNIVERSITY HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHILD; CHROMOSOME 8P; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CLINICAL EXAMINATION; DEVELOPMENTAL DISORDER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE; HUMAN; LETTER; MOTOR DYSFUNCTION; PHENOTYPE; PRIORITY JOURNAL; SPEECH DISORDER;

CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 8; DEVELOPMENTAL DISABILITIES; FEMALE; GENE DUPLICATION; HUMANS; INFANT; INVERSION, CHROMOSOME;

EID: 0032893791     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990101)82:1<91::AID-AJMG19>3.0.CO;2-E     Document Type: Letter

References (15)