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Associations between congenital heart defects and genetic and morphological anomalies. The importance of prenatal screening.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2019 Feb;163(1):67-74. doi: 10.5507/bp.2018.049. Epub 2018 Sep 6.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2019.
PMID: 30198518
Free article.
High incidence of monozygotic twinning after assisted reproduction is related to genetic information, but not to assisted reproduction technology itself.
Sobek A Jr, Zbořilová B, Procházka M, Šilhánová E, Koutná O, Klásková E, Tkadlec E, Sobek A.
Sobek A Jr, et al. Among authors: silhanova e.
Fertil Steril. 2015 Mar;103(3):756-60. doi: 10.1016/j.fertnstert.2014.12.098. Epub 2015 Jan 10.
Fertil Steril. 2015.
PMID: 25583445
Free article.
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Elejalde syndrome--a case report.
Silhánová E, Plevová P, Curík R, Kaspercík I, Krepelová A.
Silhánová E, et al.
Am J Med Genet A. 2006 Oct 15;140(20):2223-6. doi: 10.1002/ajmg.a.31419.
Am J Med Genet A. 2006.
PMID: 16969863
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Germline variants of the promyelocytic leukemia tumor suppressor gene in patients with familial cancer.
Plevova P, Walczyskova S, Jeziskova I, Jurckova N, Krepelova A, Puchmajerova A, Pavlikova K, Foretova L, Zapletalova J, Silhanova E.
Plevova P, et al. Among authors: silhanova e.
Neoplasma. 2009;56(6):500-7. doi: 10.4149/neo_2009_06_500.
Neoplasma. 2009.
PMID: 19728758
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CCND1 and ZNF217 gene amplification is equally frequent in BRCA1 and BRCA2 associated and non-BRCA breast cancer.
Plevova P, Cerna D, Balcar A, Foretova L, Zapletalova J, Silhanova E, Curik R, Dvorackova J.
Plevova P, et al. Among authors: silhanova e.
Neoplasma. 2010;57(4):325-32. doi: 10.4149/neo_2010_04_325.
Neoplasma. 2010.
PMID: 20429623
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[Single nucleotide c.645+32c>T substitution in the APC gene is a non-pathogenic polymorphism appearing in about 16% of the Czech population].
Plevová P, Drobcinská L, Stekrová J, Silhánová E.
Plevová P, et al. Among authors: silhanova e.
Cas Lek Cesk. 2008;147(5):266-8.
Cas Lek Cesk. 2008.
PMID: 18630182
Czech.
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Molecular and clinical characterization of two patients with Prader-Willi syndrome and atypical deletions of proximal chromosome 15q.
Calounova G, Hedvicakova P, Silhanova E, Kreckova G, Sedlacek Z.
Calounova G, et al. Among authors: silhanova e.
Am J Med Genet A. 2008 Aug 1;146A(15):1955-62. doi: 10.1002/ajmg.a.32416.
Am J Med Genet A. 2008.
PMID: 18627056
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