Mosaic trisomy of a small r(1) with an abnormal phenotype

American Journal of Medical Genetics

Volumn 103, Issue 1, 2001, Pages 32-35

  Dawson, A J ^a   Konkin, D ^a   Riordan, D ^a   Chudley, A E ^a  

^a UNIVERSITY OF MANITOBA   (Canada)

Author keywords

Clinical phenotype karyotype correlation; Mosaic trisomy r(1); Supernumerary marker chromosome

Indexed keywords

ARTICLE; AUTOSOME MOSAICISM; CASE REPORT; CHROMOSOME 1; CHROMOSOME BANDING PATTERN; CHROMOSOME PAINTING; CYTOGENETICS; DEVELOPMENTAL DISORDER; DISEASE SEVERITY; EUCHROMATIN; FLUORESCENCE IN SITU HYBRIDIZATION; GENE SEQUENCE; HUMAN; HUMAN CELL; KARYOTYPE; LEARNING DISORDER; MALE; MEDICAL LITERATURE; PHENOTYPE; PRIORITY JOURNAL; PROGNOSIS; RING CHROMOSOME; SCHOOL CHILD;

CHILD; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 1; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MOSAICISM; PHENOTYPE; RING CHROMOSOMES; TRISOMY;

EID: 0035885325     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1494     Document Type: Article

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