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Page 1
Preimplantation genetic testing for aneuploidy versus morphology as selection criteria for single frozen-thawed embryo transfer in good-prognosis patients: a multicenter randomized clinical trial.
Fertil Steril. 2019 Dec;112(6):1071-1079.e7. doi: 10.1016/j.fertnstert.2019.07.1346. Epub 2019 Sep 21.
Fertil Steril. 2019.
PMID: 31551155
Free article.
Clinical Trial.
A big step forward for PGT-M?
Stock-Myer S, Johnson M.
Stock-Myer S, et al.
Reprod Biomed Online. 2018 Aug;37(2):126-127. doi: 10.1016/j.rbmo.2018.06.017.
Reprod Biomed Online. 2018.
PMID: 30075839
No abstract available.
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Lymphedema distichiasis syndrome may be caused by FOXC2 promoter-enhancer dissociation and disruption of a topological associated domain.
Wallis M, Pope-Couston R, Mansour J, Amor DJ, Tang P, Stock-Myer S.
Wallis M, et al. Among authors: stock myer s.
Am J Med Genet A. 2021 Jan;185(1):150-156. doi: 10.1002/ajmg.a.61935. Epub 2020 Oct 27.
Am J Med Genet A. 2021.
PMID: 33107170
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Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro.
Natesan SA, Bladon AJ, Coskun S, Qubbaj W, Prates R, Munne S, Coonen E, Dreesen JC, Stevens SJ, Paulussen AD, Stock-Myer SE, Wilton LJ, Jaroudi S, Wells D, Brown AP, Handyside AH.
Natesan SA, et al. Among authors: stock myer se.
Genet Med. 2014 Nov;16(11):838-45. doi: 10.1038/gim.2014.45. Epub 2014 May 8.
Genet Med. 2014.
PMID: 24810687
Free PMC article.
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Three Mendelian disorders (chronic granulomatous disease, retinitis pigmentosa, ornithine transcarbamylase deficiency) in a young woman with an X chromosome deletion, del(X)(p11.4p21.1).
Coman D, Yaplito-Lee J, La P, Nasioulas S, Bruno D, Slater HR, Stock-Myer SE, Lynch EL, Gardner RJ.
Coman D, et al. Among authors: stock myer se.
Mol Genet Metab. 2010 Mar;99(3):329. doi: 10.1016/j.ymgme.2009.11.006. Epub 2009 Nov 27.
Mol Genet Metab. 2010.
PMID: 20036594
No abstract available.
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