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Marie Theresa McDonald, MD

Professor of Pediatrics
Campus mail: 2082 GSRB1, Box 103857, Durham, NC 27710
Phone: (919) 681-1982
Email address: mcdon035@mc.duke.edu

My current research interests are in the field of Clinical Genetics, Dysmorphology, and Fabry disease.

Education and Training

  • M.D., University Dublin Trinity College, 1988

Publications

Kalfa, T. A., S. A. Zimmerman, M. T. McDonald, and R. E. Ware. “Pelger-Huet anomaly in a child with 1q42.3-44 deletion.” In Pediatric Research, 53:296A-296A. INT PEDIATRIC RESEARCH FOUNDATION, INC, 2003.

Scholars@Duke

Koeberl, D. D., D. S. Millington, W. E. Smith, S. D. Weavil, J. Muenzer, S. E. McCandless, P. S. Kishnani, et al. “Evaluation of 3-methylcrotonyl-CoA carboxylase deficiency detected by tandem mass spectrometry newborn screening.” J Inherit Metab Dis 26, no. 1 (2003): 25–35. https://doi.org/10.1023/a:1024015227863.

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Golembiewski-Ruiz, V., C. A. Tirado, K. Curesky, J. Goldstein, A. McKonkie-Rosell, M. T. McDonald, and B. K. Goodman. “Cytogenetic and FISH analysis of an interstitial 1q42.3-q44 deletion.” In American Journal of Human Genetics, 71:305–305. UNIV CHICAGO PRESS, 2002.

Scholars@Duke

Wassem, Rebecca, Marie McDonald, and Janet Racine. “Fibromyalgia: patient perspectives on symptoms, symptom management, and provider utilization.” Clin Nurse Spec 16, no. 1 (January 2002): 24–28. https://doi.org/10.1097/00002800-200201000-00009.

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Erickson, R. P., S. L. Dagenais, M. S. Caulder, C. A. Downs, G. Herman, M. C. Jones, W. S. Kerstjens-Frederikse, et al. “Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations.” J Med Genet 38, no. 11 (November 2001): 761–66. https://doi.org/10.1136/jmg.38.11.761.

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Nandi, K. N., M. T. McDonald, K. K. Rogers, and K. W. Rao. “Mosaicism for two de novo supernumerary markers derived from chromosomes 18 and 13.” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 318–318.

Scholars@Duke

Glover, T. W., R. P. Erickson, S. L. Dagenais, M. T. McDonald, M. S. Caulder, B. P. Brooks, and M. W. Glynn. “Phenotypic heterogeneity in lymphedema-distichiasis with FOXC2 mutations.” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 631–631.

Scholars@Duke

Breen, C. M., K. J. Butnor, M. T. McDonald, and W. D. Bradford. “Congenital diaphragmatic defects: An autopsy case series.” Modern Pathology 14, no. 1 (January 1, 2001): 5A-5A.

Scholars@Duke

Breen, C. M., K. J. Butnor, M. T. McDonald, and W. D. Bradford. “Congenital diaphragmatic defects: An autopsy case series.” Laboratory Investigation 81, no. 1 (January 1, 2001): 5A-5A.

Scholars@Duke

Persaud, D. A., S. A. Schmidt, S. G. West, M. A. Pericak-Vance, J. M. Vance, and M. T. McDonald. “Refinement of a locus on chromosome 16q24.3 for Lymphedema-Distichiasis.” American Journal of Human Genetics 67, no. 4 (October 1, 2000): 313–313.

Scholars@Duke

Pages