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A novel EDA variant causing X-linked hypohidrotic ectodermal dysplasia: Case report.
Mol Genet Metab Rep. 2021 Sep 20;29:100796. doi: 10.1016/j.ymgmr.2021.100796. eCollection 2021 Dec.
Mol Genet Metab Rep. 2021.
PMID: 34584847
Free PMC article.
Case of Inherited Partial AZFa Deletion without Impact on Male Fertility.
Alksere B, Berzina D, Dudorova A, Conka U, Andersone S, Pimane E, Krasucka S, Blumberga A, Dzalbs A, Grinfelde I, Vedmedovska N, Fodina V, Erenpreiss J.
Alksere B, et al. Among authors: andersone s.
Case Rep Genet. 2019 Oct 31;2019:3802613. doi: 10.1155/2019/3802613. eCollection 2019.
Case Rep Genet. 2019.
PMID: 31781421
Free PMC article.
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The outcomes after transfers of embryos with chromosomal mosaicism: a single reproductive medicine center experience at iVF Riga clinic.
Alksere B, Grinfelde I, Kornejeva L, Dzalbs A, Vedmedovska N, Kovalova I, Conka U, Andersone S, Krasucka S, Blumberga A, Berzina D, Fodina V.
Alksere B, et al. Among authors: andersone s.
Gynecol Endocrinol. 2020;36(sup1):53-57. doi: 10.1080/09513590.2020.1816719.
Gynecol Endocrinol. 2020.
PMID: 33305664
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The application of PGT-A for carriers of balanced structural chromosomal rearrangements.
Fodina V, Dudorova A, Alksere B, Dzalbs A, Vedmedovska N, Andersone S, Una C, Juris E, Dace B.
Fodina V, et al. Among authors: andersone s.
Gynecol Endocrinol. 2019;35(sup1):18-23. doi: 10.1080/09513590.2019.1632091.
Gynecol Endocrinol. 2019.
PMID: 31532310
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