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pro vyhledávání: '"Bethy Jackle"'
Publikováno v:
Cancer Genetics and Cytogenetics. 138:139-142
Chronic myelocytic leukemia (CML) is a chronic myeloproliferative disorder characterized by cytogenetic or molecular evidence of Philadelphia (Ph) chromosome, t(9;22)(q34;q11). Mild to moderate eosinophilia is commonly seen in CML. However, eosinophi
Autor:
Robert G. Watts, Kelly Cox, Andrew J. Carroll, P. Nagesh Rao, Bethy Jackle, Elizabetta Abruzzese, Mary C. Steuterman, Mark J. Pettenati
Publikováno v:
Cancer Genetics and Cytogenetics. 105:164-167
We present two cases with hidden Philadelphia translocations that resulted from an insertion and a complex translocation. These cases were unusual in having the BCR/ABL fusion localized to chromosome 9q34. A review of cases with these uncommon presen
Autor:
Mark Slatkoff, Julia M. Cruz, Bethy Jackle, P. Nagesh Rao, Bayard L. Powell, Mark J. Pettenati, Elisabetta Abruzzese
Publikováno v:
Cancer Genetics and Cytogenetics. 93:140-146
Solitary loss of the X chromosome is associated with Turner syndrome and not hematological disorders. We describe five patients with non-constitutional loss of the X chromosome as the sole cytogenetic abnormality in their bone marrow. Three of the fi
Publikováno v:
Cancer genetics and cytogenetics. 138(2)
Chronic myelocytic leukemia (CML) is a chronic myeloproliferative disorder characterized by cytogenetic or molecular evidence of Philadelphia (Ph) chromosome, t(9;22)(q34;q11). Mild to moderate eosinophilia is commonly seen in CML. However, eosinophi
Autor:
Bethy Jackle, Kristin M. May, Peggy Bobby, P. Nagesh Rao, William Stewart, Chris Von Kap-Herr, Philip Mowrey, Mark J. Pettenati
Publikováno v:
American journal of medical genetics. 111(1)
Florescence in situ hybridization (FISH) using subtelomeric probes has been useful in detecting cryptic telomeric chromosomal rearrangements. We report, for the first time, that cytogenetically visible chromosome rearrangements can occur between the
Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probes
Autor:
Peggy Bobby, Philip Mowrey, Mark J. Pettenati, Jon S. Rosnes, Bethy Jackle, Chris Von Kap-Herr, Stuart Schwartz, P. Nagesh Rao
Publikováno v:
Prenatal diagnosis. 22(3)
Interphase fluorescence in situ hybridization (FISH) has become an accepted laboratory technique for the rapid and preliminary prenatal assessment of chromosome aneuploidy. The introduction of subtelomeric FISH probes now allows for the molecular-cyt