Fig. 1From: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case reportChromosome karyotype analysis of peripheral blood lymphocytes of children 1a:G-banding in metaphase of peripheral blood lymphocyte division showed chromosome karyotype 46,XY1b:G-banding in metaphase of peripheral blood lymphocyte division showed chromosome karyotype 45XY,der(15)?t(15;21),-21[26]/46,XY[24])Back to article page