B. Jackle

Monosomy X as a recurring sole cytogenetic abnormality associated with myelodysplastic diseases.

P. N. Rao, M. Pettenati, B. Powell, 1997, Cancer genetics and cytogenetics.

Chronic myelocytic leukemia with eosinophilia, t(9;12)(q34;p13), and ETV6-ABL gene rearrangement: case report and review of the literature.

Y. Keung, M. Beaty, B. Jackle, 2002, Cancer genetics and cytogenetics.

Unexpected retention and concomitant loss of subtelomeric regions in balanced chromosome anomalies by FISH.

P. N. Rao, M. Pettenati, K. May, 2002, American journal of medical genetics.

Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probes

S. Schwartz, P. Nagesh Rao, M. Pettenati, 2002, Prenatal diagnosis.

Identification of BCR-ABL fusion on chromosome 9 by fluorescence in situ hybridization in two chronic myeloid leukemia cases.

P. N. Rao, A. Carroll, M. Pettenati, 1998, Cancer genetics and cytogenetics.

Recurring translocation (10;17) and deletion (14q) in clear cell sarcoma of the kidney.

P. Koty, M. Pettenati, S. Iskandar, 2007, Archives of pathology & laboratory medicine.