Tetrasomy 15q25.3 → qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors

American Journal of Medical Genetics

Volumn 113, Issue 1, 2002, Pages 82-88

  Hu, J ^a,b   McPherson, E ^a,c,d   Surti, U ^a,d   Hasegawa, S L ^c   Gunawardena, S ^c   Gollin, S M ^a,d,e  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^c CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

^d UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

^e GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

Analphoid marker; Neocentromere; Supernumerary marker chromosome; Tetrasomy 15q; Wilms tumors

Indexed keywords

ARTICLE; CASE REPORT; CENTROMERE; CHROMOSOME 15Q; CHROMOSOME DUPLICATION; CLINICAL FEATURE; CRANIOFACIAL SYNOSTOSIS; CYTOGENETICS; FEMALE; FINGER MALFORMATION; GENOTYPE; HUMAN; HUMAN TISSUE; LYMPHOCYTE; MACROSOMIA; MARKER CHROMOSOME; NEPHROBLASTOMA; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; SKELETON MALFORMATION; SUPERNUMERARY CHROMOSOME; TETRASOMY; TUMOR CELL CULTURE;

ABNORMALITIES, MULTIPLE; ANEUPLOIDY; BONE DISEASES, DEVELOPMENTAL; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; DNA; FEMALE; HUMANS; KARYOTYPING; KIDNEY; KIDNEY NEOPLASMS; LYMPHOCYTES; WILMS TUMOR;

EID: 0037110931     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10708     Document Type: Article

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