An Adolescent with a Rare De Novo Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination

Por Peterman, Leia A., Vance, Gail H., Conboy, Erin E., Anderson, Katelynn, Weaver, David D.
Publicado no Case Rep Genet (2020)

FDA's Draft Guidance on Laboratory-Developed Tests Increases Clinical and Economic Risk to Adoption of Pharmacogenetic Testing

Por Levy, Kenneth D., Pratt, Victoria M., Skaar, Todd C., Vance, Gail H., Flockhart, David A.
Publicado no J Clin Pharmacol (2015)

Molecular Cytogenetic Analysis of Patients With Holoprosencephaly and Structural Rearrangements of 7q

Por Vance, Gail H., Nickerson, Catherine, Sarnat, Lauren, Zhang, Aiwu, Henegariu, Octavian, Morichon-Delvallez, Nicole, Butler, Merlin G., Palmer, Catherine G.
Publicado no Am J Med Genet (1998)

Report of New Haplotype for ABCC2 Gene: rs17222723 and rs8187718 in cis

Por Pratt, Victoria M., Beyer, Brittany N., Koller, Daniel L., Skaar, Todd C., Flockhart, David A., Levy, Kenneth D., Vance, Gail H.
Publicado no J Mol Diagn (2015)

Novel phenotype of 5p13.3-q11.2 duplication resulting from supernumerary marker chromosome 5: implications for management and genetic counseling

Por Armstrong, Margaret E., Weaver, David D., Lah, Melissa D., Vance, Gail H., Landis, Benjamin J., Ware, Stephanie M., Helm, Benjamin M.
Publicado no Mol Cytogenet (2018)

COMPLEMENTATION OF HYPERSENSITIVITY TO DNA INTERSTRAND CROSSLINKING AGENTS DEMONSTRATES THAT XRCC2 IS A FANCONI ANEMIA GENE

Por Park, Jung-Young, Virts, Elizabeth L., Jankowska, Anna, Wiek, Constanze, Othman, Mohamed, Chakraborty, Sujata C., Vance, Gail H., Alkuraya, Fowzan S., Hanenberg, Helmut, Andreassen, Paul R.
Publicado no J Med Genet (2016)

Interphase FISH Demonstrates that Human Adipose Stromal Cells Maintain a High Level of Genomic Stability in Long-Term Culture

Por Grimes, Brenda R., Steiner, Camie M., Merfeld-Clauss, Stephanie, Traktuev, Dmitry O., Smith, Danielle, Reese, Angela, Breman, Amy M., Thurston, Virginia C., Vance, Gail H., Johnstone, Brian H., Slee, Roger B., March, Keith L.
Publicado em 2009

Extensive Analysis of Mosaicism in a Case of Turner Syndrome: The Experience of 287 Cytogenetic Laboratories

Por Park, Jonathan P., Brothman, Arthur R., Butler, Merlin G., Cooley, Linda D., Dewald, Gordon W., Lundquist, Kurt F., Palmer, Catherine G., Patil, Shivanand R., Rao, Kathleen W., Saikevych, Irene A., Schneider, Nancy R., Vance, Gail H.
Publicado no Arch Pathol Lab Med (1999)

Genetic disruption of both Fancc and Fancg in mice recapitulates the hematopoietic manifestations of Fanconi anemia

Por Pulliam-Leath, Anna C., Ciccone, Samantha L., Nalepa, Grzegorz, Li, Xiaxin, Si, Yue, Miravalle, Leticia, Smith, Danielle, Yuan, Jin, Li, Jingling, Anur, Praveen, Orazi, Attilio, Vance, Gail H., Yang, Feng-Chun, Hanenberg, Helmut, Bagby, Grover C., Clapp, D. Wade
Publicado em 2010

Independent Prognostic Significance of Monosomy 17 and Impact of Karyotype Complexity in Monosomal Karyotype / Complex Karyotype Acute Myeloid Leukemia: Results from Four ECOG-ACRI...

Por Strickland, Stephen A, Sun, Zhuoxin, Ketterling, Rhett P, Cherry, Athena M, Cripe, Larry D, Dewald, Gordon, Fernandez, Hugo, Hicks, Gary A, Higgins, Rodney R, Lazarus, Hillard M, Litzow, Mark R, Luger, Selina M, Paietta, Elisabeth M, Rowe, Jacob M, Vance, Gail H, Wiernik, Peter, Wiktor, Anne E, Zhang, Yanming, Tallman, Martin S
Publicado no Leuk Res (2017)

Recommendations for Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guid...

Por Wolff, Antonio C., Hammond, M. Elizabeth H., Hicks, David G., Dowsett, Mitch, McShane, Lisa M., Allison, Kimberly H., Allred, Donald C., Bartlett, John M.S., Bilous, Michael, Fitzgibbons, Patrick, Hanna, Wedad, Jenkins, Robert B., Mangu, Pamela B., Paik, Soonmyung, Perez, Edith A., Press, Michael F., Spears, Patricia A., Vance, Gail H., Viale, Giuseppe, Hayes, Daniel F.
Publicado em 2013

AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia

Por Virts, Elizabeth L., Jankowska, Anna, Mackay, Craig, Glaas, Marcel F., Wiek, Constanze, Kelich, Stephanie L., Lottmann, Nadine, Kennedy, Felicia M., Marchal, Christophe, Lehnert, Erik, Scharf, Rüdiger E., Dufour, Carlo, Lanciotti, Marina, Farruggia, Piero, Santoro, Alessandra, Savasan, Süreyya, Scheckenbach, Kathrin, Schipper, Jörg, Wagenmann, Martin, Lewis, Todd, Leffak, Michael, Farlow, Janice L., Foroud, Tatiana M., Honisch, Ellen, Niederacher, Dieter, Chakraborty, Sujata C., Vance, Gail H., Pruss, Dmitry, Timms, Kirsten M., Lanchbury, Jerry S., Alpi, Arno F., Hanenberg, Helmut
Publicado no Hum Mol Genet (2015)