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Identification of iso(18p) marker chromosome by fluorescence in situ hybridization with single-copy DNA probe
H Nakashima1, T Hasegawa, M Sakai
1Department of Human Genetics, National Institute of Genetics, Mishima, Japan.
The Japanese Journal of Human Genetics
|June 1, 1995
Abstract:
The patient displayed the clinical features consistent with tetrasomy (18p) syndrome, who had an extra small metacentric iso(18p) chromosome in otherwise normal karyotype. Identification of the marker chromosome used the chromosome 18 band-specific fluorescence in situ hybridization strategy.