W. Stewart

Gastric carcinoid: germline and somatic mutation of the neurofibromatosis type 1 gene

E. Tobias, M. Balsitis, M. Upadhyaya, 2006, Familial Cancer.

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.

Fluorescence in‐Situ Hybridization on Enriched Nucleated Erythrocytes from Newborn Cord Blood

A. Sheikh, P. Rao, W. Stewart, 1994, Annals of the New York Academy of Sciences.

Jumping translocation with partial duplications and triplications of chromosomes 7 and 15

M. Pettenati, T. Jewett, K. Klinepeter, 1998, Clinical genetics.

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.

Molecular cytogenetic analysis of a duplication Xp in a male: further delineation of a possible sex influencing region on the X chromosome

P. N. Rao, R. Grubs, M. Pettenati, 1994, Human Genetics.

Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) associated with interstitial deletion of band 3q22: review and gene assignment to the interface of band 3q22.3 and 3q23.

P. N. Rao, M. Pettenati, T. Jewett, 1993, American journal of medical genetics.