Vance GH - Search Results

1

Positive and negative professionalism experiences of genetic counseling students in the United States and Canada.

Aamodt P, Wetherill L, Delk P, Torres-Martinez W, Vance GH, Wesson M. Aamodt P, et al. Among authors: vance gh. J Genet Couns. 2021 Apr;30(2):478-492. doi: 10.1002/jgc4.1334. Epub 2020 Oct 3. J Genet Couns. 2021. PMID: 33010196

2

A report of three patients with an interstitial deletion of chromosome 15q24.

Cushman LJ, Torres-Martinez W, Cherry AM, Manning MA, Abdul-Rahman O, Anderson CE, Punnett HH, Thurston VC, Sweeney D, Vance GH. Cushman LJ, et al. Among authors: vance gh. Am J Med Genet A. 2005 Aug 15;137(1):65-71. doi: 10.1002/ajmg.a.30836. Am J Med Genet A. 2005. PMID: 16007617 Review.

3

A case of de novo partial tetrasomy of distal 6p and review of the literature.

Stohler R, Kucharski E, Farrow E, Torres-Martinez W, Delk P, Thurston VC, Vance GH. Stohler R, et al. Among authors: vance gh. Am J Med Genet A. 2007 Sep 1;143A(17):1978-83. doi: 10.1002/ajmg.a.31678. Am J Med Genet A. 2007. PMID: 17663466 Review.

4

Referral patterns of Indiana oncologists for colorectal cancer genetic services.

Claybrook J, Hunter C, Wetherill LF, Vance GH. Claybrook J, et al. Among authors: vance gh. J Cancer Educ. 2010 Mar;25(1):92-5. doi: 10.1007/s13187-009-0020-2. J Cancer Educ. 2010. PMID: 20082177

5

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

Cordes Selby S, Iwata-Otsubo A, Delk P, Nebesio TD, Gohil A, Matlock P, Torres-Martinez W, Vance GH. Cordes Selby S, et al. Among authors: vance gh. Clin Case Rep. 2021 May 6;9(5):e04141. doi: 10.1002/ccr3.4141. eCollection 2021 May. Clin Case Rep. 2021. PMID: 34026173 Free PMC article.

6

Partners with reciprocal translocations: genetic counseling for the 'double translocation'.

Cook L, Hartsfield JK Jr, Vance GH. Cook L, et al. Among authors: vance gh. Clin Genet. 1998 May;53(5):403-7. doi: 10.1111/j.1399-0004.1998.tb02754.x. Clin Genet. 1998. PMID: 9660061

7

Partial trisomy 2q: report of a patient with dup (2)(q33.1q35).

Sebold CD, Romie S, Szymanska J, Torres-Martinez W, Thurston V, Muesing C, Vance GH. Sebold CD, et al. Among authors: vance gh. Am J Med Genet A. 2005 Apr 1;134A(1):80-3. doi: 10.1002/ajmg.a.30463. Am J Med Genet A. 2005. PMID: 15690398 Review.

8

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

Armstrong ME, Weaver DD, Lah MD, Vance GH, Landis BJ, Ware SM, Helm BM. Armstrong ME, et al. Among authors: vance gh. Mol Cytogenet. 2018 Mar 27;11:23. doi: 10.1186/s13039-018-0372-6. eCollection 2018. Mol Cytogenet. 2018. PMID: 29599822 Free PMC article.

9

Molecular genetic tests for FLT3, NPM1, and CEBPA in acute myeloid leukemia.

Zhang Q, Bai S, Vance GH. Zhang Q, et al. Among authors: vance gh. Methods Mol Biol. 2013;999:105-21. doi: 10.1007/978-1-62703-357-2_7. Methods Mol Biol. 2013. PMID: 23666693

10

Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicism.

Hall AL, Drendel HM, Verbrugge JL, Reese AM, Schumacher KL, Griffith CB, Weaver DD, Abernathy MP, Litton CG, Vance GH. Hall AL, et al. Among authors: vance gh. Genet Med. 2013 Sep;15(9):729-32. doi: 10.1038/gim.2013.26. Epub 2013 Mar 14. Genet Med. 2013. PMID: 23492874 Free article.

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