Delineation of supernumerary marker chromosomes in 38 patients

American Journal of Medical Genetics

Volumn 76, Issue 4, 1998, Pages 351-358

  Viersbach, Renate ^a   Engels, Hartmut ^a   Gamerdinger, Ulrike ^a   Hansmann, Manfred ^a  

^a UNIVERSITY OF BONN   (Germany)

Author keywords

Chromosomal origin; Molecular cytogenetic studies; Supernumerary marker chromosomes

Indexed keywords

ACROCENTRIC CHROMOSOME; ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 13; CHROMOSOME 14; CHROMOSOME 15; CHROMOSOME 21; CLINICAL ARTICLE; CONGENITAL MALFORMATION; FEMALE; GROWTH RETARDATION; HUMAN; INFANT; MALE; NEWBORN; PRIORITY JOURNAL; SUPERNUMERARY CHROMOSOME;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 20; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; KARYOTYPING; MALE; METAPHASE; PHENOTYPE; POLYMERASE CHAIN REACTION;

EID: 0032054591     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980401)76:4<351::AID-AJMG12>3.0.CO;2-N     Document Type: Article

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