Mosaic tetrasomy 15q25→qter in a newborn infant with multiple anomalies

American Journal of Medical Genetics

Volumn 63, Issue 3, 1996, Pages 482-485

  Van Den Enden, A ^a   Verschraegen Spae, M R ^a   Van Roy, N ^a   Decaluwe, W ^a   De Praeter, C ^a   Speleman, F ^a  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

Author keywords

chromosome 15; marker chromosome; mosaicism; tetrasomy 15q25 qter

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 15Q; CHROMOSOME MOSAICISM; CLINICAL FEATURE; CRANIOFACIAL SYNOSTOSIS; FACE MALFORMATION; FLEXION CONTRACTURE; HEART ATRIUM SEPTUM DEFECT; HUMAN; HYDRONEPHROSIS; MALE; MALFORMATION SYNDROME; MARKER CHROMOSOME; NEWBORN; PRIORITY JOURNAL; TETRASOMY;

ABNORMALITIES, MULTIPLE; ADULT; ANEUPLOIDY; CHROMOSOMES, HUMAN, PAIR 15; EAR; FACE; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KIDNEY; MALE; MOSAICISM; PREGNANCY; SKULL; TRISOMY;

EID: 0029940212     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960614)63:3<482::AID-AJMG13>3.0.CO;2-I     Document Type: Article

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