Publications by authors named "Alina Wojda"

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Truncating mutations in exons 20 and 21 of can cause primary ciliary dyskinesia without associated syndromic symptoms.
Zuzanna Bukowy-Bieryllo, Alicja Rabiasz, Maciej Dabrowski, Andrzej Pogorzelski, Alina Wojda

J Med Genet· November 2019

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: Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms Trafficking.
Ewa Zietkiewicz, Zuzanna Bukowy-Bieryllo, Alicja Rabiasz, Patrycja Daca-Roszak, Alina Wojda

Am J Respir Cell Mol Biol· October 2019

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ZMYND10--Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia.
Małgorzata Kurkowiak, Ewa Ziętkiewicz, Agnieszka Greber, Katarzyna Voelkel, Alina Wojda

PLoS One· July 2016

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Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects.
Alina Wojda, Ewa Zietkiewicz, Michał Witt

Mutagenesis· May 2007

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Correlation between the level of cytogenetic aberrations in cultured human lymphocytes and the age and gender of donors.
Alina Wojda, Ewa Zietkiewicz, Małgorzata Mossakowska, Włodzimierz Pawłowski, Krzysztof Skrzypczak

J Gerontol A Biol Sci Med Sci· August 2006

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Manifestations of ageing at the cytogenetic level.
Alina Wojda, Michał Witt

J Appl Genet· October 2003

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The 102-year old woman with translocation (7;12) and infertility in anamnesis.
Alina Wojda, Danuta Wolnik-Brzozowska, Maria Lubka, Małgorzata Mossakowska, Michał Witt

J Appl Genet· October 2003

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Infertility status of male individuals with abnormal spermiogram evaluated by cytogenetic analysis and in vitro sperm penetration assay.
Ewa Wiland, Alina Wojda, Marzena Kamieniczna, Monika Szczygieł, Maciej Kurpisz

Med Sci Monit· May 2002

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