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Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype.
Burnside RD, Pappas JG, Sacharow S, Applegate C, Hamosh A, Gadi IK, Jaswaney V, Keitges E, Phillips KK, Potluri VR, Risheg H, Smith JL, Tepperberg JH, Schwartz S, Papenhausen P. Burnside RD, et al. Among authors: potluri vr. Am J Med Genet A. 2013 Apr;161A(4):822-8. doi: 10.1002/ajmg.a.35699. Epub 2013 Mar 12. Am J Med Genet A. 2013. PMID: 23495222
Translocation (5; 11) in a conjunctival MALT lymphoma.
Clement CG, Potluri VR, Gonzales J, Qian YW. Clement CG, et al. Among authors: potluri vr. Int J Clin Exp Pathol. 2011;4(7):722-6. Epub 2011 Sep 30. Int J Clin Exp Pathol. 2011. PMID: 22076174 Free PMC article.
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.
Burnside RD, Pasion R, Mikhail FM, Carroll AJ, Robin NH, Youngs EL, Gadi IK, Keitges E, Jaswaney VL, Papenhausen PR, Potluri VR, Risheg H, Rush B, Smith JL, Schwartz S, Tepperberg JH, Butler MG. Burnside RD, et al. Among authors: potluri vr. Hum Genet. 2011 Oct;130(4):517-28. doi: 10.1007/s00439-011-0970-4. Epub 2011 Feb 27. Hum Genet. 2011. PMID: 21359847 Free PMC article.
Retinoblastoma, chromosome abnormalities and oncogene expression.
Gilbert F, Potluri VR, Short MP, Kau CL, Lalatta F. Gilbert F, et al. Among authors: potluri vr. Ophthalmic Paediatr Genet. 1987 Mar;8(1):3-10. doi: 10.3109/13816818709028508. Ophthalmic Paediatr Genet. 1987. PMID: 3295640 Review.
Chromosomal abnormalities in human retinoblastoma. A review.
Potluri VR, Helson L, Ellsworth RM, Reid T, Gilbert F. Potluri VR, et al. Cancer. 1986 Aug 1;58(3):663-71. doi: 10.1002/1097-0142(19860801)58:3<663::aid-cncr2820580311>3.0.co;2-g. Cancer. 1986. PMID: 3524791 Review.
14 results