Figure 3
From: Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl
Karyotype and chromosomal aberrations were confirmed using molecular cytogenetic approaches. (A) A deletion on derivative chromosome 9pter was identified using the subtelomeric probe 9pter; application of the probe LSI 9p21 revealed that the breakpoint in the derivative chromosome 9 was distal from 9p21; the CEP 9 probe was used as a control. (B) The application of aMCB(9) characterized the additional material on derivative as chromosome 9 derived material and characterized the duplication of chromosome 9 in more detail.