Ballif BC - Search Results

1

Modified array-based comparative genomic hybridization detects cryptic and variant PML-RARA rearrangements in acute promyelocytic leukemia lacking classic translocations.

Gruver AM, Rogers HJ, Cook JR, Ballif BC, Schultz RA, Batanian JR, Fesler MJ, Tubbs RR. Gruver AM, et al. Among authors: ballif bc. Diagn Mol Pathol. 2013 Mar;22(1):10-21. doi: 10.1097/PDM.0b013e31825b8326. Diagn Mol Pathol. 2013. PMID: 23370423

2

The use of new technologies in the detection of balanced translocations in hematologic disorders.

Shaffer LG, Schultz RA, Ballif BC. Shaffer LG, et al. Among authors: ballif bc. Curr Opin Genet Dev. 2012 Jun;22(3):264-71. doi: 10.1016/j.gde.2012.01.005. Epub 2012 Feb 13. Curr Opin Genet Dev. 2012. PMID: 22336526 Review.

3

Microarray-based comparative genomic hybridization of cancer targets reveals novel, recurrent genetic aberrations in the myelodysplastic syndromes.

Kolquist KA, Schultz RA, Furrow A, Brown TC, Han JY, Campbell LJ, Wall M, Slovak ML, Shaffer LG, Ballif BC. Kolquist KA, et al. Among authors: ballif bc. Cancer Genet. 2011 Nov;204(11):603-28. doi: 10.1016/j.cancergen.2011.10.004. Cancer Genet. 2011. PMID: 22200086

4

The use of cytogenetic microarrays in myelodysplastic syndrome characterization.

Shaffer LG, Ballif BC, Schultz RA. Shaffer LG, et al. Among authors: ballif bc. Methods Mol Biol. 2013;973:69-85. doi: 10.1007/978-1-62703-281-0_5. Methods Mol Biol. 2013. PMID: 23412784

5

Evaluation of chronic lymphocytic leukemia by oligonucleotide-based microarray analysis uncovers novel aberrations not detected by FISH or cytogenetic analysis.

Kolquist KA, Schultz RA, Slovak ML, McDaniel LD, Brown TC, Tubbs RR, Cook JR, Theil KS, Cawich V, Valentin C, Minier S, Neill NJ, Byerly S, Morton SA, Sahoo T, Ballif BC, Shaffer LG. Kolquist KA, et al. Among authors: ballif bc. Mol Cytogenet. 2011 Nov 16;4:25. doi: 10.1186/1755-8166-4-25. Mol Cytogenet. 2011. PMID: 22087757 Free PMC article.

6

Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH.

Neill NJ, Ballif BC, Lamb AN, Parikh S, Ravnan JB, Schultz RA, Torchia BS, Rosenfeld JA, Shaffer LG. Neill NJ, et al. Among authors: ballif bc. Genome Res. 2011 Apr;21(4):535-44. doi: 10.1101/gr.114579.110. Epub 2011 Mar 7. Genome Res. 2011. PMID: 21383316 Free PMC article.

7

Evaluation of chronic lymphocytic leukemia by BAC-based microarray analysis.

Schultz RA, Delioukina M, Gaal K, Bedell V, Smith DD, Forman SJ, McDaniel LD, Ballif BC, Shaffer LG, Slovak ML. Schultz RA, et al. Among authors: ballif bc. Mol Cytogenet. 2011 Feb 3;4(1):4. doi: 10.1186/1755-8166-4-4. Mol Cytogenet. 2011. PMID: 21291569 Free PMC article.

8

Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes.

Slovak ML, Smith DD, Bedell V, Hsu YH, O'Donnell M, Forman SJ, Gaal K, McDaniel L, Schultz R, Ballif BC, Shaffer LG. Slovak ML, et al. Among authors: ballif bc. Mol Cytogenet. 2010 Nov 15;3:23. doi: 10.1186/1755-8166-3-23. Mol Cytogenet. 2010. PMID: 21078186 Free PMC article.

9

Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes.

Rosenfeld JA, Drautz JM, Clericuzio CL, Cushing T, Raskin S, Martin J, Tervo RC, Pitarque JA, Nowak DM, Karolak JA, Lamb AN, Schultz RA, Ballif BC, Bejjani BA, Gajecka M, Shaffer LG. Rosenfeld JA, et al. Among authors: ballif bc. Am J Med Genet A. 2011 Aug;155A(8):1906-16. doi: 10.1002/ajmg.a.34100. Epub 2011 Jul 8. Am J Med Genet A. 2011. PMID: 21744490

10

Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes.

Rosenfeld JA, Traylor RN, Schaefer GB, McPherson EW, Ballif BC, Klopocki E, Mundlos S, Shaffer LG, Aylsworth AS; 1q21.1 Study Group. Rosenfeld JA, et al. Among authors: ballif bc. Eur J Hum Genet. 2012 Jul;20(7):754-61. doi: 10.1038/ejhg.2012.6. Epub 2012 Feb 8. Eur J Hum Genet. 2012. PMID: 22317977 Free PMC article.

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