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Page 1
Prenatal identification of partial 3q duplication syndrome.
BMC Med Genomics. 2019 Jun 13;12(1):85. doi: 10.1186/s12920-019-0547-y.
BMC Med Genomics. 2019.
PMID: 31196198
Free PMC article.
Clinical Importance of aCGH in Genetic Counselling of Children with Psychomotor Retardation.
Pasińska M, Łazarczyk E, Repczyńska A, Sobczyńska-Tomaszewska A, Zimowski J, Runge A, Haus O.
Pasińska M, et al. Among authors: runge a.
Appl Clin Genet. 2022 May 14;15:27-38. doi: 10.2147/TACG.S357136. eCollection 2022.
Appl Clin Genet. 2022.
PMID: 35603035
Free PMC article.
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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: runge a.
Genes (Basel). 2022 Apr 14;13(4):690. doi: 10.3390/genes13040690.
Genes (Basel). 2022.
PMID: 35456496
Free PMC article.
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Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the ANKRD11 Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3.
Kutkowska-Kaźmierczak A, Boczar M, Kalka E, Castañeda J, Klapecki J, Pietrzyk A, Barczyk A, Malinowska O, Landowska A, Gambin T, Kowalczyk K, Wiśniowiecka-Kowalnik B, Smyk M, Dawidziuk M, Niepokój K, Paczkowska M, Szyld P, Lipska-Ziętkiewicz B, Szczałuba K, Kostyk E, Runge A, Rutkowska K, Płoski R, Nowakowska B, Bal J, Obersztyn E, Gos M.
Kutkowska-Kaźmierczak A, et al. Among authors: runge a.
Genes (Basel). 2021 Aug 17;12(8):1257. doi: 10.3390/genes12081257.
Genes (Basel). 2021.
PMID: 34440431
Free PMC article.
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[Molecular diagnostic tests for thrombophilia in patients referred to genetic counseling clinic because due to recurrent pregnancy failure. One center's experience].
Pasińska M, Soszyńska K, Runge A, Dabrowska A, Juraszek A, Janiszewska T, Olga H.
Pasińska M, et al. Among authors: runge a.
Ginekol Pol. 2012 Mar;83(3):178-82.
Ginekol Pol. 2012.
PMID: 22568192
Polish.
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