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Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals.
Simon-Sanchez J, Scholz S, Fung HC, Matarin M, Hernandez D, Gibbs JR, Britton A, de Vrieze FW, Peckham E, Gwinn-Hardy K, Crawley A, Keen JC, Nash J, Borgaonkar D, Hardy J, Singleton A. Simon-Sanchez J, et al. Among authors: borgaonkar d. Hum Mol Genet. 2007 Jan 1;16(1):1-14. doi: 10.1093/hmg/ddl436. Epub 2006 Nov 20. Hum Mol Genet. 2007. PMID: 17116639
Y to X chromosome translocations.
Borgaonkar DS. Borgaonkar DS. Hum Genet. 1977 Dec 29;40(1):113-4. doi: 10.1007/BF00280838. Hum Genet. 1977. PMID: 564327 No abstract available.
Cytogenetic and linkage studies of a familial 15pplus variant.
Yoder FE, Bias WB, Borgaonkar DS, Bahr GF, Yoder II, Yoder OC, Golomb HM. Yoder FE, et al. Among authors: borgaonkar ds. Am J Hum Genet. 1974 Sep;26(5):535-48. Am J Hum Genet. 1974. PMID: 4138462 Free PMC article. No abstract available.
131 results