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Trisomy 13 and 18-Prevalence and mortality-A multi-registry population based analysis.
Goel N, Morris JK, Tucker D, de Walle HEK, Bakker MK, Kancherla V, Marengo L, Canfield MA, Kallen K, Lelong N, Camelo JL, Stallings EB, Jones AM, Nance A, Huynh MP, Martínez-Fernández ML, Sipek A, Pierini A, Nembhard WN, Goetz D, Rissmann A, Groisman B, Luna-Muñoz L, Szabova E, Lapchenko S, Zarante I, Hurtado-Villa P, Martinez LE, Tagliabue G, Landau D, Gatt M, Dastgiri S, Morgan M. Goel N, et al. Among authors: lapchenko s. Am J Med Genet A. 2019 Dec;179(12):2382-2392. doi: 10.1002/ajmg.a.61365. Epub 2019 Sep 30. Am J Med Genet A. 2019. PMID: 31566869 Free PMC article.
Blastopathies and microcephaly in a Chornobyl impacted region of Ukraine.
Wertelecki W, Yevtushok L, Zymak-Zakutnia N, Wang B, Sosyniuk Z, Lapchenko S, Hobart HH. Wertelecki W, et al. Among authors: lapchenko s. Congenit Anom (Kyoto). 2014 Aug;54(3):125-49. doi: 10.1111/cga.12051. Congenit Anom (Kyoto). 2014. PMID: 24666273 Free PMC article.
A teratology information system in vernacular: Closing an information gap.
Patskun E, Yevtushok L, Zymak-Zakutnia N, Lapchenko S, Akhmedzhanova D, Wertelecki W. Patskun E, et al. Among authors: lapchenko s. Birth Defects Res. 2021 Sep 1;113(15):1152-1155. doi: 10.1002/bdr2.1901. Epub 2021 Apr 24. Birth Defects Res. 2021. PMID: 33893758
EUROlinkCAT protocol for a European population-based data linkage study investigating the survival, morbidity and education of children with congenital anomalies.
Morris JK, Garne E, Loane M, Barisic I, Densem J, Latos-Bieleńska A, Neville A, Pierini A, Rankin J, Rissmann A, de Walle H, Tan J, Given JE, Claridge H; EUROlinkCAT Consortium. Morris JK, et al. BMJ Open. 2021 Jun 28;11(6):e047859. doi: 10.1136/bmjopen-2020-047859. BMJ Open. 2021. PMID: 34183346 Free PMC article.
Chornobyl, radiation, neural tube defects, and microcephaly.
Wertelecki W, Yevtushok L, Kuznietsov I, Komov O, Lapchenko S, Akhmedzanova D, Ostapchuk L. Wertelecki W, et al. Among authors: lapchenko s. Eur J Med Genet. 2018 Sep;61(9):556-563. doi: 10.1016/j.ejmg.2018.06.005. Epub 2018 Jun 13. Eur J Med Genet. 2018. PMID: 29908351
41 results