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Incidence of the 22q11.2 deletion in a large cohort of miscarriage samples.
Maisenbacher MK, Merrion K, Pettersen B, Young M, Paik K, Iyengar S, Kareht S, Sigurjonsson S, Demko ZP, Martin KA. Maisenbacher MK, et al. Among authors: merrion k. Mol Cytogenet. 2017 Mar 9;10:6. doi: 10.1186/s13039-017-0308-6. eCollection 2017. Mol Cytogenet. 2017. PMID: 28293297 Free PMC article.
Letter to the editor by megan Hall.
Saucier J, Merrion K, Mash J, Pettersen B, Hall M, Demko Z. Saucier J, et al. Among authors: merrion k. Curr Genomics. 2013 Apr;14(2):79. doi: 10.2174/1389202911314020001. Curr Genomics. 2013. PMID: 24082818 Free PMC article. No abstract available.
Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes.
Rosenfeld JA, Stephens LE, Coppinger J, Ballif BC, Hoo JJ, French BN, Banks VC, Smith WE, Manchester D, Tsai AC, Merrion K, Mendoza-Londono R, Dupuis L, Schultz R, Torchia B, Sahoo T, Bejjani B, Weaver DD, Shaffer LG. Rosenfeld JA, et al. Among authors: merrion k. Eur J Hum Genet. 2011 May;19(5):547-54. doi: 10.1038/ejhg.2010.237. Epub 2011 Jan 19. Eur J Hum Genet. 2011. PMID: 21248749 Free PMC article.