Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2019 1
2020 1
2021 1
2022 6
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

8 results

Results by year

Filters applied: . Clear all
Page 1
Ovarian tumors and genetic predisposition.
Štellmachová Júlia, Vrtěl Petr, Vrtěl Radek, Janíková Mária, Kolaříková Kristýna, Procházka Martin, Vodička Radek. Štellmachová Júlia, et al. Ceska Gynekol. 2022;87(3):211-216. doi: 10.48095/cccg2022211. Ceska Gynekol. 2022. PMID: 35896402 English.
SPG11: clinical and genetic features of seven Czech patients and literature review.
Doleckova K, Roth J, Stellmachova J, Gescheidt T, Sigut V, Houska P, Jech R, Zech M, Vyhnalek M, Vyhnalkova E, Seeman P, Meszarosova AU. Doleckova K, et al. Among authors: stellmachova j. Neurol Res. 2022 May;44(5):379-389. doi: 10.1080/01616412.2021.1975224. Epub 2022 Mar 7. Neurol Res. 2022. PMID: 35254204 Review.
Searching for genetic variants associated with thrombophilia.
Vrtěl P, Slavík L, Vodička R, Procházka M, Procházková J, Vrtěl R, Úlehlová J, Rohoň P, Štellmachová J. Vrtěl P, et al. Among authors: stellmachova j. Cas Lek Cesk. 2019 Spring;158(1):28-32. Cas Lek Cesk. 2019. PMID: 31046389 English.
Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing.
Vrtel P, Slavik L, Vodicka R, Stellmachova J, Prochazka M, Prochazkova J, Ulehlova J, Rohon P, Simurda T, Stasko J, Martinkova I, Vrtel R. Vrtel P, et al. Among authors: stellmachova j. Diagnostics (Basel). 2022 Apr 23;12(5):1060. doi: 10.3390/diagnostics12051060. Diagnostics (Basel). 2022. PMID: 35626216 Free PMC article.
Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms.
Vrtel P, Vrtel R, Klaskova E, Vrbicka D, Adamova K, Pavlicek J, Hana V, Hana V, Soucek O, Stara V, Lebl J, Snajdrova M, Zapletalova J, Furst T, Kapralova S, Tauber Z, Krejcirikova E, Routilova M, Stellmachova J, Vodicka R, Prochazka M. Vrtel P, et al. Among authors: stellmachova j. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022 Mar;166(1):63-67. doi: 10.5507/bp.2020.060. Epub 2021 Jan 12. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022. PMID: 33463629 Free article.