FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes

American Journal of Medical Genetics

Volumn 84, Issue 4, 1999, Pages 377-380

  Giardino, Daniela ^a   Bettio, D ^a   Gottardi, G ^a   Rizzi, N ^a   Pierluigi, M ^b   Perfumo, C ^b   Cali A ^b   Dagna Bricarelli, F ^b   Larizza, L ^a,b,c  

^a ISTITUTO AUXOLOGICO ITALIANO   (Italy)

^b GALLIERA HOSPITAL   (Italy)

^c UNIVERSITY OF MILAN   (Italy)

Author keywords

Chromosome 1 partial trisomy; Clinical phenotype; De novo; Marker chromosome; Supernumerary r(1)

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 1; CHROMOSOME MARKER; CHROMOSOME PAINTING; CONGENITAL MALFORMATION; CYTOGENETICS; DEVELOPMENTAL DISORDER; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE; HETEROCHROMATIN; HUMAN; HUMAN CELL; INFANT; MALE; PARTIAL TRISOMY; PHENOTYPE; PRIORITY JOURNAL; RING CHROMOSOME; SUPERNUMERARY CHROMOSOME; YEAST ARTIFICIAL CHROMOSOME;

ABNORMALITIES, MULTIPLE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; PHENOTYPE;

EID: 0033522780     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990604)84:4<377::AID-AJMG14>3.0.CO;2-U     Document Type: Article

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