Sharon L. Wenger

Education

B.A., Thiel College, 1971
M.S., University of Pittsburgh, 1973
Ph.D., University of Pittsburgh, 1976

Research

References

Wenger SL, Surti U, Nwokoro NA, Steele MW. Cytogenetic characterization of cat eye syndrome marker chromosome. Ann Genet 1994;37: 33-36.

Wenger SL, Steele MW, Boone LY, Lenkey SG, Cummins JH, Chen X-Q. "Balanced" karyotypes in six abnormal offspring of balanced reci-procal translocation normal carrier parents. Am J Med Genet 1995; 55:47-52.

Kocova M, Siegel S, Wenger SL, Lee P, Trucco M. Detection of Y chromosome sequences in a 45,X/46,XXq- patient by Southern blot of PCR-amplified DNA and fluorescent in situ hybridization (FISH). Am J Med Genet 1995;55:483-488.

Scott JA, Wenger SL, Steele MW, Chakravarti A. Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation. Am J Med Genet 1995;56:67-71.

Wenger SL. Chemical induction of sister chromatid exchange at fragile sites. Cancer Genet Cytogenet 1995;85:72-74.

Olinsky S, Loop BT, DeKosky A, Ripepi B, Weng W, Cummins J, Wenger SL, Yan Y, Langenaur C, Narayanan V. Chromosomal mapping of the human M6 genes. Genomics 1996;33:532-536.

Greally JM, Neiswanger K, Cummins JH, Boone LY, Lenkey SG, Wenger SL, Lewis JL, Fischer D, Paul RA, Steele MW. A molecular anatomical analysis of mosaic trisomy 16. Hum Genet 1996;98:86-90.

Wenger SL, Giangreco CA, Tarleton J, Wessel HB. Inability to induce fragile sites at CTG repeats in congenital myotonic dystrophy. Am J Med Genet 1996;66:60-63.