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Page 1
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome.
Genes (Basel). 2023 Mar 9;14(3):680. doi: 10.3390/genes14030680.
Genes (Basel). 2023.
PMID: 36980952
Free PMC article.
Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies.
Kowalczyk K, Bartnik-Głaska M, Smyk M, Plaskota I, Bernaciak J, Kędzior M, Wiśniowiecka-Kowalnik B, Deperas M, Domaradzka J, Łuszczek A, Dutkiewicz D, Kozar A, Grad D, Niemiec M, Ziemkiewicz K, Magdziak R, Braun-Walicka N, Barczyk A, Geremek M, Castañeda J, Kutkowska-Kaźmierczak A, Własienko P, Jakubów-Durska K, Dębska M, Kucińska-Chahwan A, Kozłowski S, Mikulska B, Issat T, Roszkowski T, Nawara-Baran A, Runge A, Jakubiuk-Tomaszuk A, Kruczek A, Kostyk E, Pietras G, Limon J, Zwoliński J, Ochman K, Szajner T, Węgrzyn P, Wielgoś M, Sąsiadek M, Obersztyn E, Nowakowska BA.
Kowalczyk K, et al. Among authors: ziemkiewicz k.
Genes (Basel). 2022 Apr 14;13(4):690. doi: 10.3390/genes13040690.
Genes (Basel). 2022.
PMID: 35456496
Free PMC article.
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Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability.
Bartnik M, Nowakowska B, Derwińska K, Wiśniowiecka-Kowalnik B, Kędzior M, Bernaciak J, Ziemkiewicz K, Gambin T, Sykulski M, Bezniakow N, Korniszewski L, Kutkowska-Kaźmierczak A, Klapecki J, Szczałuba K, Shaw CA, Mazurczak T, Gambin A, Obersztyn E, Bocian E, Stankiewicz P.
Bartnik M, et al. Among authors: ziemkiewicz k.
J Appl Genet. 2014 Feb;55(1):125-44. doi: 10.1007/s13353-013-0181-x. Epub 2013 Dec 3.
J Appl Genet. 2014.
PMID: 24297458
Free PMC article.
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Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors.
Hochstenbach R, Nowakowska B, Volleth M, Ummels A, Kutkowska-Kaźmierczak A, Obersztyn E, Ziemkiewicz K, Gerloff C, Schanze D, Zenker M, Muschke P, Schanze I, Poot M, Liehr T.
Hochstenbach R, et al. Among authors: ziemkiewicz k.
Mol Syndromol. 2016 Feb;6(5):210-21. doi: 10.1159/000441408. Epub 2015 Oct 31.
Mol Syndromol. 2016.
PMID: 26997941
Free PMC article.
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Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling?
Jezela-Stanek A, Pokora P, Młynek M, Smyk M, Ziemkiewicz K, Różdżyńska-Świątkowska A, Tylki-Szymańska A.
Jezela-Stanek A, et al. Among authors: ziemkiewicz k.
Clin Dysmorphol. 2021 Apr 1;30(2):76-82. doi: 10.1097/MCD.0000000000000344.
Clin Dysmorphol. 2021.
PMID: 33290290
Free PMC article.
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Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders.
Bartnik M, Szczepanik E, Derwińska K, Wiśniowiecka-Kowalnik B, Gambin T, Sykulski M, Ziemkiewicz K, Kędzior M, Gos M, Hoffman-Zacharska D, Mazurczak T, Jeziorek A, Antczak-Marach D, Rudzka-Dybała M, Mazurkiewicz H, Goszczańska-Ciuchta A, Zalewska-Miszkurka Z, Terczyńska I, Sobierajewicz M, Shaw CA, Gambin A, Mierzewska H, Mazurczak T, Obersztyn E, Bocian E, Stankiewicz P.
Bartnik M, et al. Among authors: ziemkiewicz k.
Am J Med Genet B Neuropsychiatr Genet. 2012 Oct;159B(7):760-71. doi: 10.1002/ajmg.b.32081. Epub 2012 Jul 23.
Am J Med Genet B Neuropsychiatr Genet. 2012.
PMID: 22825934
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[Clinical manifestation of chromosome 2 long arm terminal deletion--presentation of four cases].
Szczałuba K, Obersztyn E, Ziemkiewicz K, Jamsheer A, Bocian E, Mazurczak T.
Szczałuba K, et al. Among authors: ziemkiewicz k.
Med Wieku Rozwoj. 2007 Jan-Mar;11(1):57-64.
Med Wieku Rozwoj. 2007.
PMID: 17965466
Polish.
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