Trkova M - Search Results

1

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: trkova m. Gene. 2013 Mar 1;516(1):158-61. doi: 10.1016/j.gene.2012.12.027. Epub 2012 Dec 22. Gene. 2013. PMID: 23266801

2

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: trkova m. Cytogenet Genome Res. 2012;136(1):15-20. doi: 10.1159/000334709. Epub 2011 Dec 8. Cytogenet Genome Res. 2012. PMID: 22156400

3

Association of 17q24.2-q24.3 deletions with recognizable phenotype and short telomeres.

Hancarova M, Malikova M, Kotrova M, Drabova J, Trkova M, Sedlacek Z. Hancarova M, et al. Among authors: trkova m. Am J Med Genet A. 2018 Jun;176(6):1438-1442. doi: 10.1002/ajmg.a.38711. Epub 2018 Apr 25. Am J Med Genet A. 2018. PMID: 29696806

4

A 15 Mb large paracentric chromosome 21 inversion identified in Czech population through a pair of flanking duplications.

Drabova J, Trkova M, Hancarova M, Novotna D, Hejtmankova M, Havlovicova M, Sedlacek Z. Drabova J, et al. Among authors: trkova m. Mol Cytogenet. 2014 Aug 19;7:51. doi: 10.1186/1755-8166-7-51. eCollection 2014. Mol Cytogenet. 2014. PMID: 25411581 Free PMC article.

5

Expanded DMPK repeats in dizygotic twins referred for diagnosis of autism versus absence of expanded DMPK repeats at screening of 330 children with autism.

Musova Z, Hancarova M, Havlovicova M, Pourova R, Hrdlicka M, Kraus J, Trkova M, Stejskal D, Sedlacek Z. Musova Z, et al. Among authors: trkova m. Neuropsychiatr Dis Treat. 2016 Sep 19;12:2367-2372. doi: 10.2147/NDT.S113917. eCollection 2016. Neuropsychiatr Dis Treat. 2016. PMID: 27695335 Free PMC article.

6

Increased sperm aneuploidy in two male carriers of germline TP53 mutations.

Paulasova P, Diblik J, Trkova M, Macek M Sr, Sedlacek Z. Paulasova P, et al. Among authors: trkova m. Cancer Genet. 2011 May;204(5):278-81. doi: 10.1016/j.cancergen.2011.03.003. Cancer Genet. 2011. PMID: 21665182

7

Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?

Trkova M, Hladikova M, Kasal P, Goetz P, Sedlacek Z. Trkova M, et al. J Hum Genet. 2002;47(8):381-6. doi: 10.1007/s100380200055. J Hum Genet. 2002. PMID: 12181637

8

A Li-Fraumeni syndrome family with retained heterozygosity for a germline TP53 mutation in two tumors.

Trkova M, Foretova L, Kodet R, Hedvicakova P, Sedlacek Z. Trkova M, et al. Cancer Genet Cytogenet. 2003 Aug;145(1):60-4. doi: 10.1016/s0165-4608(03)00031-1. Cancer Genet Cytogenet. 2003. PMID: 12885464

9

Analysis of genetic events in 17p13 and 9p21 regions supports predominant monoclonal origin of multifocal and recurrent bladder cancer.

Trkova M, Babjuk M, Duskova J, Benesova-Minarikova L, Soukup V, Mares J, Minarik M, Sedlacek Z. Trkova M, et al. Cancer Lett. 2006 Oct 8;242(1):68-76. doi: 10.1016/j.canlet.2005.10.036. Epub 2005 Dec 15. Cancer Lett. 2006. PMID: 16343743

10

Telomere length in peripheral blood cells of germline TP53 mutation carriers is shorter than that of normal individuals of corresponding age.

Trkova M, Prochazkova K, Krutilkova V, Sumerauer D, Sedlacek Z. Trkova M, et al. Cancer. 2007 Aug 1;110(3):694-702. doi: 10.1002/cncr.22834. Cancer. 2007. PMID: 17567834 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

46 results

Search Page

Filters