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primeFISH Products               Prenatal
                                                                                      PRENATAL

                                                                                              PANEL



                                                                       1002-CXY Chr X/Y DC Probe Kit



          For cases of chronic myeloid leukemia (CML) in individuals   The centromeric X/Y probe can detect abnormal copy
          who undergo allogeneic bone marrow transplantation   numbers of the X and Y chromosomes. Numerical anom-
          from the opposite sex, interphase nuclei and metaphase   alies associated with the sex chromosomes can lead to
          spreads obtained from bone marrow samples are indi-  various conditions. For example, Klinefelter syndrome
          cated for additional use in standard cytogenetic analysis   (47,XXY), Turner syndrome (45,X), and other chromosomal
          to identify and count the X and Y chromosomes using   disorders are syndromes caused by changes in the copy
          FISH. The centromeric X/Y probe is not designed for use   numbers of X and/or Y chromosomes. These syndromes
          in subjects who have the same sex for bone marrow   have variable incidences and clinical manifestations.
          transplantation.

























                                                    DXZ1
                                                    Xp11.1-q11.1










                                                        DYZ3
                                                     Yp11.1-q11.1







                                                  (Not to scale)



                                                                                             References

                                                                          Bryndorf et al. (1996) Am J Hum Genet 59:918-926
                                                                           Tepperberg et al. (2001) Prenat Diagn 21:293-301  www.diagen.com.tr
                                                                            Tsuchiya KD. (2011) Clin Lab Med. 31(4):525-42.
                                                                           Rickman L, et al. (2006) J Med Genet 43:353-361.





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