A case of 3q29 microdeletion with novel features and a review of cytogenetically visible terminal 3q deletions

Clinical Dysmorphology

Volumn 15, Issue 3, 2006, Pages 145-148

  Baynam, Gareth ^a,b   Goldblatt, Jack ^a   Townshend, Sharron ^a  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^b Genetic Services of Western Australia   (Australia)

Author keywords

3q29 deletions; 3qter deletions; Subtelomeric deletions

Indexed keywords

ADOLESCENT; ASPERGER SYNDROME; CASE REPORT; CHROMOSOME 3Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL FEATURE; CONTRACTURE; GROWTH DISORDER; HUMAN; LUMBAR VERTEBRA; MALE; PHENOTYPE; PRIORITY JOURNAL; REVIEW; VEIN THROMBOSIS; CHROMOSOME 3; CONGENITAL MALFORMATION; CRANIOFACIAL MALFORMATION; DEVELOPMENTAL DISORDER; GENETICS; KARYOTYPING; LANGUAGE DISABILITY; LEARNING DISORDER; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 3; CRANIOFACIAL ABNORMALITIES; DEVELOPMENTAL DISABILITIES; HUMANS; KARYOTYPING; LANGUAGE DEVELOPMENT DISORDERS; LEARNING DISORDERS; LUMBAR VERTEBRAE; MALE;

EID: 33748202535     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.mcd.0000198934.55071.ee     Document Type: Review

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