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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. Mol Cytogenet. 2017 Mar 9;10:6. doi: 10.1186/s13039-017-0308-6. eCollection 2017. Mol Cytogenet. 2017. PMID: 28293297 Free PMC article.
Novel ploidy analysis in ectopic pregnancy.
Ruderman RS, McQueen DB, Robins JC, Barnhart KT, Maisenbacher MK, Feinberg EC. Ruderman RS, et al. Among authors: maisenbacher mk. F S Rep. 2020 Nov 18;2(1):67-71. doi: 10.1016/j.xfre.2020.11.002. eCollection 2021 Mar. F S Rep. 2020. PMID: 34223275 Free PMC article.
Neutropenia in Barth syndrome: characteristics, risks, and management.
Steward CG, Groves SJ, Taylor CT, Maisenbacher MK, Versluys B, Newbury-Ecob RA, Ozsahin H, Damin MK, Bowen VM, McCurdy KR, Mackey MC, Bolyard AA, Dale DC. Steward CG, et al. Among authors: maisenbacher mk. Curr Opin Hematol. 2019 Jan;26(1):6-15. doi: 10.1097/MOH.0000000000000472. Curr Opin Hematol. 2019. PMID: 30451719 Free PMC article. Clinical Trial.
Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion.
Saitta SC, Harris SE, Gaeth AP, Driscoll DA, McDonald-McGinn DM, Maisenbacher MK, Yersak JM, Chakraborty PK, Hacker AM, Zackai EH, Ashley T, Emanuel BS. Saitta SC, et al. Among authors: maisenbacher mk. Hum Mol Genet. 2004 Feb 15;13(4):417-28. doi: 10.1093/hmg/ddh041. Epub 2003 Dec 17. Hum Mol Genet. 2004. PMID: 14681306 Free PMC article.
27 results