Two cases with partial trisomy 9p: Molecular cytogenetic characterization and clinical follow-up

American Journal of Medical Genetics

Volumn 109, Issue 2, 2002, Pages 125-132

  Littooij, Annemieke S ^a   Hochstenbach, Ron ^a   Sinke, Richard J ^a   Van Tintelen, Peter ^b   Giltay, Jacques C ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

Author keywords

DNA marker analysis; Fluorescence in situ hybridization; Reciprocal translocation; Trisomy 14q; Trisomy 9p

Indexed keywords

DNA MARKER;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 9P; CLINICAL EXAMINATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; PARTIAL TRISOMY 9; PHENOTYPE; PRIORITY JOURNAL; RECIPROCAL CHROMOSOME TRANSLOCATION;

CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; FOLLOW-UP STUDIES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; KARYOTYPING; MICROSATELLITE REPEATS; TRANSLOCATION, GENETIC; TRISOMY;

EID: 0037156313     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10322     Document Type: Article

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