Mosaic tetrasomy 9p in a girl with multiple congenital anomalies: Cytogenetic and molecular-cytogenetic studies

European Journal of Pediatrics

Volumn 158, Issue 7, 1999, Pages 571-575

  Stumm, M ^b   Tonnies H ^a   Mandon, U ^a   Gotze A ^b   Krebs, P ^b   Wieacker, P F ^b  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b UNIVERSITY HOSPITAL MAGDEBURG   (Germany)

Author keywords

Comparative genomic hybridisation; Fluorescence in situ hybridisation; Tetrasomy 9p

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 9P; CHROMOSOME MOSAICISM; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MALFORMATION SYNDROME; PRIORITY JOURNAL; TETRASOMY;

ABNORMALITIES, MULTIPLE; ADOLESCENT; BLINDNESS; BONE AND BONES; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 9; CRANIOFACIAL ABNORMALITIES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MENTAL RETARDATION; MOSAICISM; NUCLEIC ACID HYBRIDIZATION; SENSITIVITY AND SPECIFICITY;

EID: 0033041237     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310051149     Document Type: Article

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