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

door Peterman, Leia A., Vance, Gail H., Conboy, Erin E., Anderson, Katelynn, Weaver, David D.
Gepubliceerd in Case Rep Genet (2020)

FDA's Draft Guidance on Laboratory-Developed Tests Increases Clinical and Economic Risk to Adoption of Pharmacogenetic Testing

door Levy, Kenneth D., Pratt, Victoria M., Skaar, Todd C., Vance, Gail H., Flockhart, David A.
Gepubliceerd in J Clin Pharmacol (2015)

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

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

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

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

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

door Armstrong, Margaret E., Weaver, David D., Lah, Melissa D., Vance, Gail H., Landis, Benjamin J., Ware, Stephanie M., Helm, Benjamin M.
Gepubliceerd in 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

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

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

door 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.
Gepubliceerd in J Med Genet (2016)

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

door 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.
Gepubliceerd in 2009

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

door 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.
Gepubliceerd in Arch Pathol Lab Med (1999)

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

door 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
Gepubliceerd in 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...

door 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
Gepubliceerd in 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...

door 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.
Gepubliceerd in 2013

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

door 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
Gepubliceerd in Hum Mol Genet (2015)