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Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility.
Wang JC, Ross L, Mahon LW, Owen R, Hemmat M, Wang BT, El Naggar M, Kopita KA, Randolph LM, Chase JM, Matas Aguilera MJ, Siles JL, Church JA, Hauser N, Shen JJ, Jones MC, Wierenga KJ, Jiang Z, Haddadin M, Boyar FZ, Anguiano A, Strom CM, Sahoo T. Wang JC, et al. Among authors: anguiano a. Eur J Hum Genet. 2015 May;23(5):663-71. doi: 10.1038/ejhg.2014.153. Epub 2014 Aug 13. Eur J Hum Genet. 2015. PMID: 25118026 Free PMC article.
Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangements.
Sahoo T, Wang JC, Elnaggar MM, Sanchez-Lara P, Ross LP, Mahon LW, Hafezi K, Deming A, Hinman L, Bruno Y, Bartley JA, Liehr T, Anguiano A, Jones M. Sahoo T, et al. Among authors: anguiano a. Eur J Hum Genet. 2015 Jan;23(1):61-6. doi: 10.1038/ejhg.2014.53. Epub 2014 Apr 9. Eur J Hum Genet. 2015. PMID: 24713661 Free PMC article.
Neocentric X-chromosome in a girl with Turner-like syndrome.
Hemmat M, Wang BT, Warburton PE, Yang X, Boyar FZ, El Naggar M, Anguiano A. Hemmat M, et al. Among authors: anguiano a. Mol Cytogenet. 2012 Jun 9;5(1):29. doi: 10.1186/1755-8166-5-29. Mol Cytogenet. 2012. PMID: 22682421 Free PMC article.
Submicroscopic deletion of 5q involving tumor suppressor genes (CTNNA1, HSPA9) and copy neutral loss of heterozygosity associated with TET2 and EZH2 mutations in a case of MDS with normal chromosome and FISH results.
Hemmat M, Chen W, Anguiano A, Naggar ME, Racke FK, Jones D, Wang Y, Strom CM, Chang K, Boyar FZ. Hemmat M, et al. Among authors: anguiano a. Mol Cytogenet. 2014 May 27;7:35. doi: 10.1186/1755-8166-7-35. eCollection 2014. Mol Cytogenet. 2014. PMID: 25177364 Free PMC article.
38 results