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

Year Number of Results
2005 1
2006 1
2007 3
2008 3
2009 3
2010 2
2011 1
2012 1
2013 1
2015 1
2016 2
2017 5
2018 2
2019 5
2020 3
2021 3
2022 2
2024 0

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34 results

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Page 1
Post-zygotic diploidization of triploidy in human is possible? - a case of triploid partial molar pregnancy resulting in a premature live-born diploid female infant.
Kosinska-Kaczynska K, Dabrowski FA, Mazanowska N, Kosiński P, Skórka A, Kostrzewa G, Michalak E, Górnicka B, Płaza O, Zgliczynska M, Wielgos M. Kosinska-Kaczynska K, et al. Among authors: kostrzewa g. Neuro Endocrinol Lett. 2019 Dec;40(5):227-232. Neuro Endocrinol Lett. 2019. PMID: 32112547 Review.
Neurodevelopmental disorder associated with IRF2BPL gene mutation: Expanding the phenotype?
Skorvanek M, Dusek P, Rydzanicz M, Walczak A, Kosinska J, Kostrzewa G, Brzozowska M, Han V, Dosekova P, Gdovinova Z, Lehotska Z, Lisowski P, Ploski R. Skorvanek M, et al. Among authors: kostrzewa g. Parkinsonism Relat Disord. 2019 May;62:239-241. doi: 10.1016/j.parkreldis.2019.01.017. Epub 2019 Jan 24. Parkinsonism Relat Disord. 2019. PMID: 30733140 No abstract available.
Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins-Diagnostic implications.
Rydzanicz M, Olszewski P, Kedra D, Davies H, Filipowicz N, Bruhn-Olszewska B, Cavalli M, Szczałuba K, Młynek M, Machnicki MM, Stawiński P, Kostrzewa G, Krajewski P, Śladowski D, Chrzanowska K, Dumanski JP, Płoski R. Rydzanicz M, et al. Among authors: kostrzewa g. Mol Genet Genomic Med. 2021 Jan;9(1):e1526. doi: 10.1002/mgg3.1526. Epub 2020 Dec 14. Mol Genet Genomic Med. 2021. PMID: 33319479 Free PMC article.
KIR2DS5 in the presence of HLA-C C2 protects against endometriosis.
Nowak I, Płoski R, Barcz E, Dziunycz P, Kamiński P, Kostrzewa G, Milewski Ł, Roszkowski PI, Senitzer D, Malejczyk J, Kuśnierczyk P. Nowak I, et al. Among authors: kostrzewa g. Immunogenetics. 2015 Apr;67(4):203-9. doi: 10.1007/s00251-015-0828-3. Epub 2015 Mar 1. Immunogenetics. 2015. PMID: 25724317 Free PMC article.
Novel COL12A1 variant as a cause of mild familial extracellular matrix-related myopathy.
Jezela-Stanek A, Walczak A, Łaźniewski M, Kosińska J, Stawiński P, Murcia Pienkowski V, Biernacka A, Rydzanicz M, Kostrzewa G, Krajewski P, Plewczyński D, Płoski R. Jezela-Stanek A, et al. Among authors: kostrzewa g. Clin Genet. 2019 Jun;95(6):736-738. doi: 10.1111/cge.13534. Epub 2019 Mar 28. Clin Genet. 2019. PMID: 30920656 No abstract available.
34 results