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864-250-7949, ext.
102 (voice)
864-250-9582 (fax)
crogers@ggc.org |
Senior Clinical Geneticist - Greenville
- M.D., Medical University of South Carolina, 1980
- Resident (Pediatrics), Greenville Hospital System, Greenville,
SC, 1983
- Fellow (Clinical Genetics), Greenwood Genetic Center,
Greenwood, SC, 1985
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As Director of the Greenville Office of the Greenwood Genetic
Center, Dr. Rogers is responsible for clinical genetics services
in Upstate South Carolina. With four genetic counselors (three in Greenville
and one in Spartanburg) and three clinical geneticists, the Greenville Office provides a wide range of services
which encompass every age group. These services include:
- Clinical evaluations of infants, children, and adults who
have malformations and/or mental retardation.
- Prenatal/preconceptional counseling for women with advanced
maternal age, abnormal maternal serum screening, drug or medication
exposures, or a know family history of malformations or mental
retardation.
Dr. Rogers has a special interest in the etiology and clinical
aspects of skeletal dysplasias and craniofacial anomalies. He is also a
clinician with the XLMR evaluation and research team.
Selected Publications:
- Rogers RC et al. Tricho-rhino-phalangeal syndrome
with exostoses (Langer-Giedion syndrome). Proc Greenwood Genet
Cntr 6:44-47, 1987.
- Phelan MC, Rogers RC, et al. Cytogenetic, biochemical,
and molecular analysis of a 22q13 deletion. Am J Med Genet 43:872-876,
1992.
- Saul RA, Rogers RC, et al. Brachmann-de Lange
syndrome: Diagnostic difficulties posed by the mild phenotype. Am J Med Genet
47:999-1002, 1993.
- Phelan MC, Rogers RC, et al. Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals.
Am J Med Genet 58:1-7, 1995.
- Anderson WG, Rogers RC. Hand-foot-uterus syndrome
versus ulnar-mammary syndrome - A patient with overlapping phenotypic
features. Proc Greenwood Genet Cntr 14:17-20, 1995.
- Robson WML, Leung AKC, Rogers RC. Unilateral renal
agenesis. Adv Pediatr 42:575-592, 1995.
- Brown A, Phelan MC, Patil S, Crawford EC, Rogers RC,
Schwartz C. Two patients with duplication of 17p11.2: The reciprocal
of the Smith-Magenis deletion? Am J Med Genet 63:373-377, 1996.
- Rogers RC, Houk C, Jones SJ, Blackburn W. Lethal skeletal
dysplasias. Proc Greenwood Genet Cntr 16:58-68, 1997.
- Graham JM, Tackels D, Dibbern K, Superneau D, Rogers RC,
et al: FG syndrome. Report of three new families with linkage to Xq12-q22.1.
Am J Med Genet 80:145-56, 1998.
- Graham JM, Superneau D, Rogers RC, et al. Clinical
and behavioral characteristics in FG syndrome. Am J Med Genet 85:470-475,
1999.
- Hane BG, Rogers RC and Schwartz C. Germline
mosaicism in X-linked myotubular myopathy. Clin Genet 56:77-81, 1999.
- Boyadjiev SA, Jabs EW, LaBuda M, Jamal JE, Torbergsen T,
Ptacek LJ, Rogers RC, et al. Linkage analysis narrows the critical
region for oculodentodigital dysplasia to chromosome 6q22-q23. Genomics
58:34-40, 1999.
- Phelan MC, Rogers RC, Saul RA, Stapleton GA, Sweet
K, McDermid H, Shaw SR, Claytor J, Willis J, Kelly DP. 22q13 deletion
syndrome. Am J Med Genet 101:91-9, 2001.
- Phelan MC, Rogers RC, et al. Velocardiofacial
syndrome in an unexplained XX male. Am J Med Genet 116:77-9, 2003.
- de Mollerat XJ, Everman DB, Morgan CT, Clarkson KB,
Rogers RC, et al. P63 mutations are not a major cause of non-syndromic
split hand/foot malformation. J Med Genet 40:55-61, 2003.
- Rogers RC: Detection of a
3-beta-hydroxysteroid-delta(8)delta(7) isomerase (emapomil binding protein)
mutation in a patient with chondrodysplasia punctata. Proc Greenwood Genetic
Center 17-22, 2003.
- Phelan MC. Stapleton GA, Rogers RC. Terminal
22q13 deletion syndrome. In: Management of Genetic Syndromes, ed 2.
Wiley-Liss, Inc., New York, 2005.
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