De novo mosaic add(3) characterized to be trisomy 14q31-qter using spectral karyotyping and subtelomeric probes

American Journal of Medical Genetics

Volumn 82, Issue 4, 1999, Pages 318-321

  Reddy, Kavita S ^a   Sulcova, V ^a   Young, H ^b   Blancato, J K ^b   Haddad, B R ^b,c  

^a QUEST DIAGNOSTICS NICHOLS INSTITUTE   (United States)

^b Research Institute for Genetic and Human Therapy   (United States)

^c GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Mosaic trisomy 14q31 qter

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 14Q; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPING; MOSAICISM; PRIORITY JOURNAL; TRISOMY;

ADULT; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 13; DEVELOPMENTAL DISABILITIES; FEMALE; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MENTAL RETARDATION; MOSAICISM; PHENOTYPE; TRISOMY;

EID: 0033590672     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990212)82:4<318::AID-AJMG8>3.0.CO;2-0     Document Type: Article

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