G. Velagaleti

Validation of primed in situ labeling (PRINS) for interphase analysis: comparative studies with conventional fluorescence in situ hybridization and chromosome analyses.

G. Velagaleti, S. A. Tharapel, A. Tharapel, 1999, Cancer genetics and cytogenetics.

Chromosome duplications and deletions and their mechanisms of origin

R. Michaelis, G. Velagaleti, S. A. Tharapel, 1999, Cytogenetic and Genome Research.

Rapid identification of marker chromosomes using primed in situ labeling (PRINS).

G. Velagaleti, S. A. Tharapel, A. Tharapel, 1997, American journal of medical genetics.

Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysis.

R. Michaelis, S. Lewin, G. Velagaleti, 1997, American journal of medical genetics.

Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.

K. Hirschhorn, P. Warburton, R. Mahmood, 2002, American journal of medical genetics.

Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.

S. R. Rose, E. Pivnick, G. Velagaleti, 1996, Journal of medical genetics.