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864-941-8129
(voice)
864-941-8133 (fax)
hataylor@ggc.org |
Emeritus Laboratory Geneticist
- B.S. (1965), MS (1967), Ph.D. (1971), University of Tennessee,
Knoxville
- Postdoctoral Fellow, Department of Pediatrics, Johns Hopkins
University School of Medicine, Baltimore, MD, 1971-1973
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Director, Diagnostic Laboratories, Greenwood Genetic Center,
Greenwood, SC, 1974-2008
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Selected Publications:
- Phelan MC, Thomas GR, Saul RA, Rogers RC, Taylor HA,
Wenger DA, McDermid HE. Cytogenetic, biochemical, and molecular
analyses of a 22q13 deletion. Am J Med Genet 43:872-6, 1992.
- Taylor HA and Skinner SA. Beta-Galactosidase deficiency.
Proc Greenwood Genet Cntr 12:19-22, 1993.
- Taylor HA and Thomas GA. Pseudodeficiency of alpha-iduronidase.
J Inher Metab Dis 16:1058-9, 1993.
- Kaye EM, Shalish C, Livermore BS, Taylor HA,
Stevenson RE, Breakfield XO. ß-Galactosidase gene mutations in
patients with slowly progressive Gm1 gangliosidosis. J Child
Neurol 12:242-7, 1997.
- Taylor HA, Rogers C, Jones A, Blouin R: Missed
diagnosis of maple syrup urine disease presenting as a psychiatric disorder.
Proc Greenwood Genetic Center 20:48-50, 2001.
- Wood TC, Flannery D, Kottra J, Longshore J,
Taylor HA: Biochemical and molecular analysis of a patient with congenital
disorder of glycosylation type 1a. Glycobiology 11:906A, 2001.
- Hahn KA, Salomons GA, Tackels-Horne D, Wood TC, Taylor HA, Schroer
RJ, Lubs HA, Jakobs C, Olson RL, Holden KR, Stevenson RE, Schwartz CE: X-linked mental retardation with seizures and carrier
manifestations is caused by a mutation in the creatine transporter gene
(SLC6A8) located in Xq28. Am J Hum Genet 70:1349-1356, 2002.
- Wood TC, Olson RL, Hahn KA, Salomons GS, Tackels-Horne
D, Holden KR, Taylor HA, Schroer RJ, Stevenson RE, Schwartz CE: Identification of creatine transporter deficiency in a large X-linked
mental retardation (XLMR) family. Presented at Annual Meeting of Society of
Inherited Metabolic Disorders, 2002.
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