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[Mutations in genes affecting fertility of men - current routine laboratory genetic diagnostics and searching for more DNA segments and genes influencing spermatogenesis].
Ceska Gynekol. 2016 Winter;81(6):437-443.
Ceska Gynekol. 2016.
PMID: 27918162
Czech.
Recurrent Microdeletions at Xq27.3-Xq28 and Male Infertility: A Study in the Czech Population.
Chylíková B, Hrdlička I, Veselá K, Řežábek K, Liška F.
Chylíková B, et al. Among authors: hrdlicka i.
PLoS One. 2016 Jun 3;11(6):e0156102. doi: 10.1371/journal.pone.0156102. eCollection 2016.
PLoS One. 2016.
PMID: 27257673
Free PMC article.
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[Dilemma of the results interpretation of molecular genetic analysis with a focus on CFTR gene mutations in men with reproductive disorders and in gamete donors].
Hrdlicka I.
Hrdlicka I.
Ceska Gynekol. 2008 Dec;73(6):323-7.
Ceska Gynekol. 2008.
PMID: 19170365
Czech.
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Patterns of deletions and the distribution of breakpoints in the dystrophin gene in Czech patients with Duchenne and Becker muscular dystrophy (statistical comparison with results from several other countries).
Hrdlicka I, Zadina J, Krejcí R, Srbová A, Kucerová M.
Hrdlicka I, et al.
Folia Biol (Praha). 2001;47(3):81-7.
Folia Biol (Praha). 2001.
PMID: 11409318
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NOTCH2NLC CGG Repeats Are Not Expanded and Skin Biopsy Was Negative in an Infantile Patient With Neuronal Intranuclear Inclusion Disease.
Jedlickova I, Pristoupilova A, Hulkova H, Vrbacka A, Stranecky V, Hruba E, Jesina P, Honzik T, Hrdlicka I, Fremuth J, Pivovarcikova K, Bitar I, Matej R, Kmoch S, Sikora J.
Jedlickova I, et al. Among authors: hrdlicka i.
J Neuropathol Exp Neurol. 2020 Oct 1;79(10):1065-1071. doi: 10.1093/jnen/nlaa070.
J Neuropathol Exp Neurol. 2020.
PMID: 32827029
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