Proximal interstitial 6q deletion: A recognizable syndrome

American Journal of Medical Genetics

Volumn 71, Issue 3, 1997, Pages 353-356

  Kumar, R ^a   Riordan, D ^a   Dawson, A J ^a   Chudley, A E ^a  

^a CHILDREN S HOSPITAL RESEARCH INSTITUTE OF MANITOBA   (Canada)

Author keywords

Birth defects; Chromosome anomaly; Connective tissue dysplasia; Interstitial deletion; Mental retardation

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 6Q; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DISEASE COURSE; GENE DELETION; HUMAN; HUMAN CELL; HUMAN TISSUE; INTERSTITIAL CHROMOSOME DELETION; MALE; PRIORITY JOURNAL; SCHOOL CHILD; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 6; COLLAGEN DISEASES; FACE; HUMANS; MALE; MENTAL RETARDATION; PHENOTYPE; SYNDROME;

EID: 0030747987     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970822)71:3<353::AID-AJMG18>3.0.CO;2-J     Document Type: Article

References (10)