Fig. 2
From: Small supernumerary marker chromosomes derived from chromosome 14 and/or 22
The 291/355 cases with clear clinical result studied herein are subdivided by normal and abnormal phenotypes. In first column all 291 cases are listed (14/22—all), the second and third columns include only sSMCs derived from chromosomes 14 or 22, i.e. der(14) or der(22), respectively; the last column includes unresolvable cases (14/22—unres). Normal cases are highlighted in blue, abnormal in red