Trisomy first, translocation second, uniparental disomy and partial trisomy third: A new mechanism for complex chromosomal aneuploidy

European Journal of Human Genetics

Volumn 5, Issue 5, 1997, Pages 308-314

  Schinzel, Albert ^a   Kotzot, Dieter ^a   Brecevic, Lukrecija ^a   Robinson, Wendy P ^a   Dutly, Fabrizio ^a   Dauwerse, Hans ^b   Binkert, Franz ^a   Baumer, Alessandra ^a   Ausserer, Bernd ^c  

^a UNIVERSITY OF ZURICH   (Switzerland)

^b LEIDEN UNIVERSITY   (Netherlands)

^c Hospital of Dornbirn   (Austria)

Author keywords

Mosaicism; Trisomy 16p; Uniparental disomy

Indexed keywords

ANEUPLOIDY; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 16P; CHROMOSOME 1P; CHROMOSOME MOSAICISM; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GROWTH RETARDATION; HUMAN; HUMAN CELL; HYPOSPADIAS; KIDNEY DYSPLASIA; MALE; MATERNAL AGE; MICROCEPHALY; NORMAL HUMAN; PARTIAL TRISOMY; PRIORITY JOURNAL; SHORT STATURE; UNIPARENTAL DISOMY;

EID: 0030733443     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000484782     Document Type: Article

References (16)

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