Kebrdlova V - Search Results

1

New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease.

Stekrova J, Reiterova J, Svobodova S, Kebrdlova V, Lnenicka P, Merta M, Viklicky O, Kohoutova M. Stekrova J, et al. Among authors: kebrdlova v. BMC Med Genet. 2009 Aug 17;10:78. doi: 10.1186/1471-2350-10-78. BMC Med Genet. 2009. PMID: 19686598 Free PMC article.

2

Molecular analysis of the APC and MYH genes in Czech families affected by FAP or multiple adenomas: 13 novel mutations.

Vandrovcová J, Stekrová J, Kebrdlová V, Kohoutová M. Vandrovcová J, et al. Among authors: kebrdlova v. Hum Mutat. 2004 Apr;23(4):397. doi: 10.1002/humu.9224. Hum Mutat. 2004. PMID: 15024739

3

The influence of endothelin-A receptor gene polymorphism on the progression of autosomal dominant polycystic kidney disease and IgA nephropathy.

Reiterová J, Merta M, Stekrová J, Maixnerová D, Obeidová H, Kebrdlová V, Viklický O, Tesar V. Reiterová J, et al. Among authors: kebrdlova v. Folia Biol (Praha). 2007;53(4):134-7. Folia Biol (Praha). 2007. PMID: 17706018 Free article.

4

PKD2 mutations in a Czech population with autosomal dominant polycystic kidney disease.

Stekrová J, Reiterová J, Merta M, Damborsky J, Zidovská J, Kebrdlová V, Kohoutová M. Stekrová J, et al. Among authors: kebrdlova v. Nephrol Dial Transplant. 2004 May;19(5):1116-22. doi: 10.1093/ndt/gfh083. Epub 2004 Feb 19. Nephrol Dial Transplant. 2004. PMID: 14993477

5

Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.

Stekrova J, Sulova M, Kebrdlova V, Zidkova K, Kotlas J, Ilencikova D, Vesela K, Kohoutova M. Stekrova J, et al. Among authors: kebrdlova v. BMC Med Genet. 2007 Apr 5;8:16. doi: 10.1186/1471-2350-8-16. BMC Med Genet. 2007. PMID: 17411426 Free PMC article.

6

Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families.

Schwarzová L, Štekrová J, Florianová M, Novotný A, Schneiderová M, Lněnička P, Kebrdlová V, Kotlas J, Veselá K, Kohoutová M. Schwarzová L, et al. Among authors: kebrdlova v. Fam Cancer. 2013 Mar;12(1):35-42. doi: 10.1007/s10689-012-9569-8. Fam Cancer. 2013. PMID: 22987206

7

Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients.

Sulová M, Zídková K, Kleibl Z, Stekrová J, Kebrdlová V, Bortlík M, Lukás M, Kohoutová M. Sulová M, et al. Among authors: kebrdlova v. Eur J Cancer. 2007 Jul;43(10):1617-21. doi: 10.1016/j.ejca.2007.04.010. Epub 2007 May 23. Eur J Cancer. 2007. PMID: 17524638

8

Cryptic chromosomal rearrangements in children with idiopathic mental retardation in the Czech population.

Hirschfeldova K, Baxova A, Kebrdlova V, Solc R, Mihalova R, Lnenicka P, Vesela K, Stekrova J. Hirschfeldova K, et al. Among authors: kebrdlova v. Genet Test Mol Biomarkers. 2011 Sep;15(9):607-11. doi: 10.1089/gtmb.2010.0218. Epub 2011 Apr 7. Genet Test Mol Biomarkers. 2011. PMID: 21473681

9

Detection of SHOX gene aberrations in routine diagnostic practice and evaluation of phenotype scoring form effectiveness.

Hirschfeldova K, Florianova M, Kebrdlova V, Urbanova M, Stekrova J. Hirschfeldova K, et al. Among authors: kebrdlova v. J Hum Genet. 2017 Feb;62(2):253-257. doi: 10.1038/jhg.2016.117. Epub 2016 Oct 6. J Hum Genet. 2017. PMID: 27708272

10

[Hereditary forms of colorectal adenomatous polyposis].

Kohoutová M, Stekrová J, Sulová M, Zidková K, Kleibl Z, Vandrovcová J, Kebrdlová V, Kotlas J, Jirásek V. Kohoutová M, et al. Among authors: kebrdlova v. Cas Lek Cesk. 2006;145(6):475-9. Cas Lek Cesk. 2006. PMID: 16836001 Czech.

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