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Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes.
Andrology. 2020 Mar;8(2):434-441. doi: 10.1111/andr.12704. Epub 2019 Nov 22.
Andrology. 2020.
PMID: 31479588
Free article.
Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism.
Grzesiuk JD, Pereira CS, Grangeiro CH, Picanço-Albuquerque CG, Oliveira-Gennaro FG, Machado FB, Medina-Acosta E, Ramos ES, Yoshimoto M, Martelli L.
Grzesiuk JD, et al.
Mol Cytogenet. 2016 Jun 15;9:45. doi: 10.1186/s13039-016-0249-5. eCollection 2016.
Mol Cytogenet. 2016.
PMID: 27313662
Free PMC article.
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Erratum to: Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism.
Grzesiuk JD, Pereira CS, Grangeiro CH, Picanço-Albuquerque CG, Oliveira-Gennaro FG, Machado FB, Medina-Acosta E, Ramos ES, Yoshimoto M, Martelli L.
Grzesiuk JD, et al.
Mol Cytogenet. 2016 Jul 5;9:53. doi: 10.1186/s13039-016-0262-8. eCollection 2016.
Mol Cytogenet. 2016.
PMID: 27382416
Free PMC article.
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Identification of a rare copy number polymorphic gain at 3q12.2 with candidate genes for familial endometriosis.
Oliveira FG, Rosa-E-Silva JC, Gomes AG, Grzesiuk JD, Vidotto T, Squire JA, Panepucci RA, Meola J, Martelli L.
Oliveira FG, et al. Among authors: grzesiuk jd.
Rev Bras Ginecol Obstet. 2024 Mar 15;46:e-rbgo12. doi: 10.61622/rbgo/2024CR12. eCollection 2024.
Rev Bras Ginecol Obstet. 2024.
PMID: 38765507
Free PMC article.
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