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864-250-7949, ext.
104 (voice)
864-250-9582 (fax)
gail@ggc.org |
Senior Clinical Genetic Counselor
- B.S. (Biology), Furman University, Greenville, South
Carolina, 1989
- M.S. (Genetic
Counseling), University of South Carolina, Columbia, SC, 1997
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Gail has been with the Greenwood Genetic Center since 1989,
first as a genetic caseworker and now as a genetic counselor.
She works primarily in pediatrics and has a special interest in working with
support groups. Gail serves on the board of the National 22q13 Deletion Syndrome
Foundation. She coordinates and facilitates parent groups for Fragile X
syndrome, Angelman syndrome, and Rett syndrome, and serves as facilitator for
the Muscular Dystrophy Association's family network.
Selected Publications:
- Schwartz CE, May M, Huang T, Ledbetter D, Anderson G,
Barker DF, Lubs HA, Arena F, and Stevenson RE. MRX8: An X-linked
mental retardation condition with linkage to Xq21. Am J Med Genet,
43:467-474, 1992.
- Rogers RC and Anderson G. Hand-Foot-Uterus syndrome
versus Ulnar-Mammary syndrome in a patient with overlapping phenotypic
features. Proc. Greenwood Genet Cntr, 14:17-20, 1995.
- Anderson G, Schroer RJ, Stevenson RE. Mental Retardation
in South Carolina II: Causation. Proc. Greenwood Genet Cntr,
15:32-44, 1996.
- Anderson G. Inherited Mental
Retardation: The Fragile X Syndrome. In: Biology A Community Context (suppl).
South-Western Eduational Publishing, 1998.
- Anderson G. The Journey
Through Grief. Newsletter of the National Angelman Syndrome Foundation, Volume
11 No. 1, Spring 1999.
- Stapleton GA and Rogers
RC. Neonatal Marfan Syndrome with an Affected Parent. Proc Greenwood Genetic
Cntr 19:38-39, 2000.
- Dupont B, Stapleton G, Terawaki H, and Chapman S.
Prenatal Diagnosis of Jacobsen Syndrome. Presented at the 2000 meeting of The
American Society of Human Genetics, Philadelphia, Pennsylvania, October 2000.
Am J Hum Genet 67:422, 2000.
- Stapleton GA and Lander L. Working With Support
Groups. Perspectives in Genetic Counseling, Volume 22 No. 2, Summer 2000.
- McDermid H, Yse Y, Stapleton G, and Wilson H.
Molecular Characterization of the 22q13 Deletion Syndrome. Presented at the
23rd meeting of the American Society of Human Genetics, San Diego, CA, October
2001. Am J Hum Genet 68:434, 2001.
- Stapleton GA. Incorporating Support Groups as a Part
of Genetic Services: One Center’s Experience. Proc Greenwood Genetic Cntr
20:39-43, 2001.
- Wilson HL, Wong ACC, Shaw SR, Tse W-Y, Stapleton GA,
Phelan MC, Hu S, Marshall J, McDermid HE. Molecular Characterization of the
22q13 Deletion Syndrome Supports the Role of Haploinsufficiency of
SHANK3/PROSAP2 in the Major Neurological Symptoms. J Med Genet 40:1-10, 2003.
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