Kristin G. Monaghan

Cytogenetic and clinical findings in a patient with a deletion of 16q23.1: first report of bilateral cataracts and a 16q deletion.

G. Feldman, K. Monaghan, D. V. Van Dyke, 1997, American journal of medical genetics.

Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.

C. Gunter, A. Reiss, S. Warren, 2000, American journal of human genetics.

Mutation analysis of the cystic fibrosis and cationic trypsinogen genes in patients with alcohol-related pancreatitis.

G. Feldman, C. Jackson, D. Kukuruga, 2000, American journal of medical genetics.