Cri du chat syndrome after preimplantation genetic diagnosis for reciprocal translocation Yinghui Ye, M.D., Ph.D., Yuqin Luo, B.Sc., Yuli Qian, B.Sc., Chenming Xu, Ph.D., Fan Jin, M.D. Fertility and Sterility Volume 96, Issue 1, Pages e71-e75 (July 2011) DOI: 10.1016/j.fertnstert.2011.04.080 Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions
Figure 1 Karyotype of the child with Emanuel syndrome [47,XY, + der(22) t(11; 22)(q23;q11.2)]. Fertility and Sterility 2011 96, e71-e75DOI: (10.1016/j.fertnstert.2011.04.080) Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions
Figure 2 Karyotype of the mother [46,XX, t(11;22)(q23;q11.2)]. Fertility and Sterility 2011 96, e71-e75DOI: (10.1016/j.fertnstert.2011.04.080) Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions
Figure 3 Fluorescent in situ hybridization image of embryo with normal/balanced signal. Fertility and Sterility 2011 96, e71-e75DOI: (10.1016/j.fertnstert.2011.04.080) Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions
Figure 4 Karyotype of the child with cri du chat syndrome [46,XY, del(5)(p15.2) t(11;22)(q23;q11.2)]. Fertility and Sterility 2011 96, e71-e75DOI: (10.1016/j.fertnstert.2011.04.080) Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions