Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISH

Clinical Dysmorphology

Volumn 9, Issue 1, 2000, Pages 55-57

  Petek, Erwin ^a   Köstl, Gerhard ^b   Mutz, Ingomar ^b   Wagner, Klaus ^a   Kroisel, Peter Michael ^a  

^a UNIVERSITY OF GRAZ   (Austria)

^b Leoben Hospital   (Austria)

Author keywords

Chromosome microdissection; Fluorescence in situ hybridization (FISH); Microcephaly; Trisomy 22q13 qter

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 22Q; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HYPOGONADISM; MALE; MENTAL DEFICIENCY; MICROCEPHALY; MICROPHTHALMIA; MOTOR RETARDATION; PARTIAL TRISOMY; PRIORITY JOURNAL; SCHOOL CHILD;

EID: 0033971639     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200009010-00011     Document Type: Article

References (12)

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