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

av Peterman, Leia A., Vance, Gail H., Conboy, Erin E., Anderson, Katelynn, Weaver, David D.
I publikationen Case Rep Genet (2020)

FDA's Draft Guidance on Laboratory-Developed Tests Increases Clinical and Economic Risk to Adoption of Pharmacogenetic Testing

av Levy, Kenneth D., Pratt, Victoria M., Skaar, Todd C., Vance, Gail H., Flockhart, David A.
I publikationen J Clin Pharmacol (2015)

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

av Vance, Gail H., Nickerson, Catherine, Sarnat, Lauren, Zhang, Aiwu, Henegariu, Octavian, Morichon-Delvallez, Nicole, Butler, Merlin G., Palmer, Catherine G.
I publikationen Am J Med Genet (1998)

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

av Pratt, Victoria M., Beyer, Brittany N., Koller, Daniel L., Skaar, Todd C., Flockhart, David A., Levy, Kenneth D., Vance, Gail H.
I publikationen J Mol Diagn (2015)

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

av Armstrong, Margaret E., Weaver, David D., Lah, Melissa D., Vance, Gail H., Landis, Benjamin J., Ware, Stephanie M., Helm, Benjamin M.
I publikationen Mol Cytogenet (2018)

A brother and sister with the same karyotype: Case report of two siblings with partial 3p duplication and partial 9p deletion and sex reversal

av Cordes Selby, Susan, Iwata‐Otsubo, Aiko, Delk, Paula, Nebesio, Todd D., Gohil, Anisha, Matlock, Peggy, Torres‐Martinez, Wilfredo, Vance, Gail H.
I publikationen Clin Case Rep (2021)

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

av 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.
I publikationen J Med Genet (2016)

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

av 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.
Publicerad 2009

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

av 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.
I publikationen Arch Pathol Lab Med (1999)

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

av 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
Publicerad 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...

av 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
I publikationen 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...

av 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.
Publicerad 2013

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

av 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
I publikationen Hum Mol Genet (2015)