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Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing.
Eur J Pediatr. 2016 Sep;175(9):1199-1207. doi: 10.1007/s00431-016-2759-x. Epub 2016 Aug 18.
Eur J Pediatr. 2016.
PMID: 27539621
Late onset of familial neurogenic diabetes insipidus in monozygotic twins.
Cizmarova M, Nagyova G, Janko V, Pribilincova Z, Virgova D, Ilencikova D, Kovacs L.
Cizmarova M, et al.
Endocr Regul. 2013 Oct;47(4):211-6. doi: 10.4149/endo_2013_04_211.
Endocr Regul. 2013.
PMID: 24156710
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New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype Correlations.
Čizmárová M, Hlinková K, Bertok S, Kotnik P, Duba HC, Bertalan R, Poločková K, Košťálová Ľ, Pribilincová Z, Hlavatá A, Kovács L, Ilenčíková D.
Čizmárová M, et al.
Ann Hum Genet. 2016 Jan;80(1):50-62. doi: 10.1111/ahg.12140. Epub 2015 Nov 26.
Ann Hum Genet. 2016.
PMID: 26607044
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Rasopathies - dysmorphic syndromes with short stature and risk of malignancy.
Cizmarova M, Kostalova L, Pribilincova Z, Lasabova Z, Hlavata A, Kovacs L, Ilencikova D.
Cizmarova M, et al.
Endocr Regul. 2013 Oct;47(4):217-22. doi: 10.4149/endo_2013_04_217.
Endocr Regul. 2013.
PMID: 24156711
Review.
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[Clinical dysmorphic syndromes with tumorigenesis].
Ilenčíková D, Cižmárová M, Krajčiová A, Požgayová S, Rybárová A, Kovács L.
Ilenčíková D, et al. Among authors: cizmarova m.
Klin Onkol. 2012;25 Suppl:S39-48.
Klin Onkol. 2012.
PMID: 22920206
Review.
Slovak.
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