Sedlacek Z - Search Results

1

Monozygotic twins with 17q21.31 microdeletion syndrome.

Vlckova M, Hancarova M, Drabova J, Slamova Z, Koudova M, Alanova R, Mannik K, Kurg A, Sedlacek Z. Vlckova M, et al. Among authors: sedlacek z. Twin Res Hum Genet. 2014 Oct;17(5):405-10. doi: 10.1017/thg.2014.29. Epub 2014 Jun 9. Twin Res Hum Genet. 2014. PMID: 24909117

2

Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism.

Vazna A, Havlovicova M, Sedlacek Z. Vazna A, et al. Among authors: sedlacek z. Gene. 2008 Jan 15;407(1-2):186-92. doi: 10.1016/j.gene.2007.10.009. Epub 2007 Oct 13. Gene. 2008. PMID: 17996402

3

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: sedlacek z. 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

4

FMR1 gene expansion, large deletion of Xp, and skewed X-inactivation in a girl with mental retardation and autism.

Vazna A, Musova Z, Vlckova M, Novotna D, Dvorakova L, Hrdlicka M, Havlovicova M, Sedlacek Z. Vazna A, et al. Among authors: sedlacek z. Am J Med Genet A. 2010 May;152A(5):1273-7. doi: 10.1002/ajmg.a.33352. Am J Med Genet A. 2010. PMID: 20425835

5

Array comparative genome hybridization in patients with developmental delay: two example cases.

Hancarova M, Drabova J, Zmitkova Z, Vlckova M, Hedvicakova P, Novotna D, Vlckova Z, Vejvalkova S, Marikova T, Sedlacek Z. Hancarova M, et al. Among authors: sedlacek z. N Biotechnol. 2012 Feb 15;29(3):321-4. doi: 10.1016/j.nbt.2010.10.006. Epub 2010 Oct 20. N Biotechnol. 2012. PMID: 20969982

6

Mechanism and genotype-phenotype correlation of two proximal 6q deletions characterized using mBAND, FISH, array CGH, and DNA sequencing.

Vlckova M, Trkova M, Zemanova Z, Hancarova M, Novotna D, Raskova D, Puchmajerova A, Drabova J, Zmitkova Z, Tan Y, Sedlacek Z. Vlckova M, et al. Among authors: sedlacek z. Cytogenet Genome Res. 2012;136(1):15-20. doi: 10.1159/000334709. Epub 2011 Dec 8. Cytogenet Genome Res. 2012. PMID: 22156400

7

Skin lesions in a boy with X-linked lymphoproliferative disorder: comparison of 5 SH2D1A deletion cases.

Mejstríková E, Janda A, Hrusák O, Bucková H, Vlcková M, Hancárová M, Freiberger T, Ravcuková B, Vesely K, Fajkusová L, Kopecková L, Sumerauer D, Kabícková E, Sedivá A, Stary J, Sedlácek Z. Mejstríková E, et al. Among authors: sedlacek z. Pediatrics. 2012 Feb;129(2):e523-8. doi: 10.1542/peds.2011-0870. Epub 2012 Jan 23. Pediatrics. 2012. PMID: 22271700

8

Identification of a patient with intellectual disability and de novo 3.7 Mb deletion supports the existence of a novel microdeletion syndrome in 2p14-p15.

Hancarova M, Vejvalkova S, Trkova M, Drabova J, Dleskova A, Vlckova M, Sedlacek Z. Hancarova M, et al. Among authors: sedlacek z. Gene. 2013 Mar 1;516(1):158-61. doi: 10.1016/j.gene.2012.12.027. Epub 2012 Dec 22. Gene. 2013. PMID: 23266801

9

Chromosome 12q13.13 deletions involving the HOXC gene cluster: phenotype and candidate genes.

Hancarova M, Simandlova M, Drabova J, Petrak B, Koudova M, Havlovicova M, Sedlacek Z. Hancarova M, et al. Among authors: sedlacek z. Eur J Med Genet. 2013 Mar;56(3):171-3. doi: 10.1016/j.ejmg.2012.12.003. Epub 2012 Dec 27. Eur J Med Genet. 2013. PMID: 23274590 No abstract available.

10

A patient with de novo 0.45 Mb deletion of 2p16.1: the role of BCL11A, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome.

Hancarova M, Simandlova M, Drabova J, Mannik K, Kurg A, Sedlacek Z. Hancarova M, et al. Among authors: sedlacek z. Am J Med Genet A. 2013 Apr;161A(4):865-70. doi: 10.1002/ajmg.a.35783. Epub 2013 Mar 12. Am J Med Genet A. 2013. PMID: 23495096

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