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Journal of the Association of Genetic Technologists|December 16, 2005
Cell death as a possible mechanism for tissue limited mosaicism in Pallister-Killian syndromeWozhan Tang, Sharon L WengerThe Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 9, 2004
Cleft palate in a newborn with duplication 2(q13q23)Sharon L Wenger, Ona C Bleigh, Marybeth HummelJournal of the Association of Genetic Technologists|March 17, 2012
Patterns of BCR/ABL Gene Rearrangements in Chronic Myeloid Leukemia with Complex t(9;22) Using Fluorescence In Situ Hybridization (FISH)Olukemi A Esan, Jamie R Senft, Sharon L WengerJournal of the Association of Genetic Technologists|June 24, 2004
Partial 7q Isochromosome in Bone Marrow Following Treatment of Hodgkin's DiseasePhilip S. Grove, Miklos L. Auber, Sharon L. WengerJournal of the Association of Genetic Technologists|July 20, 2005
Extra copy of 20q deletion, acute myelomonocytic leukemia (M4) and Niemann-Pick diseaseDana M Wonsettler, William W L Chang, Sharon L WengerJournal of the Association of Genetic Technologists|February 24, 2010
Case report: cytogenetic and molecular analysis of proximal interstitial deletion of 4p, review of the literature and comparison with wolf-hirschhorn syndromeNathanael G Bailey, Sarah T South, Marybeth Hummel, et al.International Journal of Surgical Pathology|May 30, 2008
Del(5q) is associated with clinical and histological parameters in small cell neuroendocrine lung carcinomaPaul H Hartel, Amy L Shackelford, James V Hartel, et al.American Journal of Medical Genetics. Part A|April 12, 2005
Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotypeViktoria N Evdokimova, Reagan K McLoughlin, Sharon L Wenger, et al.Molecular Cancer Therapeutics|December 19, 2006
Fanconi anemia D2 protein confers chemoresistance in response to the anticancer agent, irofulvenYutian Wang, Timothy Wiltshire, Jamie Senft, et al.Prenatal Diagnosis|October 19, 2005
Prenatal detection of deletion 6q13q15 in a complex karyotypeMin Yu, Angela C Obringer, Melissa H Fowler, et al.Pageof 3