Authors: MONAGHAN KG RYBICKI BA SHURAFA M FELDMAN GL

Citation: Kg. Monaghan et al., MUTATION ANALYSIS OF THE HFE GENE ASSOCIATED WITH HEREDITARY HEMOCHROMATOSIS IN AFRICAN-AMERICANS, American journal of hematology, 58(3), 1998, pp. 213-217

Authors: MONAGHAN KG DENNEHY PJ VANDYKE DL WEISS L

Citation: Kg. Monaghan et al., BILATERAL PETERS ANOMALY IN AN INFANT WITH 49,XXXXY SYNDROME, Journal of pediatric ophthalmology and strabismus, 35(2), 1998, pp. 112-113

Authors: MONAGHAN KG VANDYKE DL FELDMAN GL

Citation: Kg. Monaghan et al., PRADER-WILLI-LIKE-SYNDROME IN A PATIENT WITH AN XQ23Q25 DUPLICATION, American journal of medical genetics, 80(3), 1998, pp. 227-231

Authors: MONAGHAN KG VANDYKE DL WIKTOR A FELDMAN GL

Citation: Kg. Monaghan et al., CYTOGENETIC AND CLINICAL FINDINGS IN A PATIENT WITH A DELETION OF 16Q23.1 - FIRST REPORT OF BILATERAL CATARACTS AND A 16Q DELETION, American journal of medical genetics, 73(2), 1997, pp. 180-183

Authors: MONAGHAN KG RYBICKI B SHURAFA M FELDMAN GL

Citation: Kg. Monaghan et al., MUTATION ANALYSIS OF THE HLA-H GENE ASSOCIATED WITH HEREDITARY HEMOCHROMATOSIS IN AFRICAN-AMERICANS, American journal of human genetics, 61(4), 1997, pp. 2262-2262

Authors: MONAGHAN KG VANDYKE DL FELDMAN G WIKTOR A WEISS L

Citation: Kg. Monaghan et al., DIAGNOSTIC TESTING - A COST-ANALYSIS FOR PRADER-WILLI AND ANGELMAN SYNDROMES, American journal of human genetics, 60(1), 1997, pp. 244-247