Page 8 - DIAGEN
P. 8

Hermatology  primeFISH Products


              HEMATOLOGY

              PANEL



              17-054 del(7q31.2)



              Chromosome 7 monosomy and deletion of the long arm of   (AML), and juvenile myelomonocytic leukemia (JMML).
              chromosome 7 are recurrent chromosomal abnormalities   The pres  ence of Monosomy 7 or del (7q) as karyotypic
              frequently seen in myeloid diseases. Monosomy 7 and   changes is associated with worse out  comes in myeloid
              de1(7q); it is seen in many myeloid diseases, including   malignancies.
              myelodysplastic syndrome (MDS), acute myeloid leukemia






















                                                                              DELETION






                     D7Z1
                     (7p11.1-q11.1)                                             NORMAL







                                    D7S486       STSG597801                    DELETION
                                             3'  5'
                     7q31.2      Gen                    Tel
                                            TES
                                            358 kb


                                    (Not to scale)





      www.diagen.com.tr  References
              Fisher et al., Blood 1997;89(6):2036-2041
              Arsham, MS., Barch, MJ. and Lawce HJ. (eds.) (2017) The AGT Cytogenetics Laboratory Manual. New Jersey: John Wiley & Sons Inc.
              Trobaugh-Lotrario et al., Bone Marrow Transplantation 2005;35(2):143-149





       8      PRODUCT CATALOGUE     info@diagen.com.tr
   3   4   5   6   7   8   9   10   11   12   13