검색어 : 통합검색[657.5]
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- 657del5 Mutation of the Nijmegen Breakage Syndrome Gene (NBS1) in the Turkish Population
- Tekin, Mustafa; Akcayoz, Duygu; Ucar, Canan; Gulen, Huseyin; Akar, Nejat; ; (Human biology, v.77, 2005, pp.393-397)
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- Regional distribution of heterozygous 657del5 mutation carriers of theNBS1 gene in Wielkopolska province (Poland)
- Zió łkowska, Iwona; Mosor, Maria; Nowak, Jerzy; ; (Journal of applied genetics, v.47, 2006, pp.269-272)
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- Carrier frequency of mutation 657del5 in the <i>NBS1</i> gene in a population of polish pediatric patients with sporadic lymphoid malignancies
- Chrzanowska, Krystyna H.; Piekutowska‐ Abramczuk, Dorota; Popowska, Ewa; Gładkowska‐ Dura, Małgorzata; Małdyk, Jadwiga; Syczewska, Małgorzata; Krajewska‐ Walasek, Małgorzata; Goryluk‐ Kozakiewicz, Boż enna; Bubała, Halina; Gadomski, Artur; Gaworczyk, Anna; Kazanowska, Bernarda; Kołtan, Andrzej; Kuź micz, Marta; Luszawska‐ Kutrzeba, Teresa; Maciejka‐ Kapuś ciń ska, Lucyna; Stolarska, Małgorzata; Stefań ska, Katarzyna; Sznurkowska, Katarzyna; Wakuliń ska, Anna; Wieczorek, Maria; Szczepań ski, Tomasz; Kowalczyk, Jerzy; Department of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland; Department of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland; Department of Pathology, Children's Memorial Health Institute, Warsaw, Poland; Department of Pathology, Medical University of Warsaw, Warsaw, Poland; Department of Rehabilitation, Children's Memorial Health Institute, Warsaw, Poland; Department of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland; Department of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland; Department of Pediatric Hematology and Oncology, Silesian Academy of Medicine, Zabrze, Poland; Department of Pediatric Hematology and Oncology, Medical University of Warsaw, Warsaw, Poland; Department of Pediatric H; (International journal of cancer: Journal international du cancer, v.118, 2006, pp.1269-1274)
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- The interface in carbon fibre composites - Piggot, M.R. Carbon Vol 27 No 5 pp 657-662
- ; ; (Composites, v.21, 1990, pp.269)
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- Gardiner, Mary S. The principles of general biology. New York: The Macmillan Company, 1952. 657 P. $5.25
- ; ; (Science education, v.38, 1954, pp.313-313)
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- The hot corrosion of in-657 superalloy in Na<sub>2</sub>SO<sub>4</sub>-V<sub>2</sub>O<sub>5</sub> melt eutectic
- Otero, E.; Pardo, A.; Herná ez, J.; Pé rez, F.J.; Departamento de Cí encia de Materiales, Facultad de Quimica, Universidad Complutense, 28040 Madrid, Spain; Departamento de Cí encia de Materiales, Facultad de Quimica, Universidad Complutense, 28040 Madrid, Spain; Departamento de Cí encia de Materiales, Facultad de Quimica, Universidad Complutense, 28040 Madrid, Spain; Departamento de Cí encia de Materiales, Facultad de Quimica, Universidad Complutense, 28040 Madrid, Spain; (Corrosion science, v.32, 1991, pp.677-683)
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- Market for Ethical Drugs Grew 3.5% to Yen7,345,657 Mil. in FY2004: IMS Japan
- ; ; (Pharma Japan: Japan drug industry news, v.1946, 2005, pp.4)
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- A 100kW Forced-Air-Cooled SiC MOSFET Converter Achieving a Power Density of 1.657kW/L and an Efficiency over 98.5%
- Zhang, Lei; Li, Yan; Zhang, Yonglei; Yuan, Xibo; Wang, Zijian; Li, Zhe; China University of Mining and Technology, School of Electrical and Power Engineering, Xuzhou, China; China University of Mining and Technology, School of Electrical and Power Engineering, Xuzhou, China; China University of Mining and Technology, School of Electrical and Power Engineering, Xuzhou, China; University of Bristol, School of Electrical and Power Engineering, Bristol, United Kingdom; China University of Mining and Technology, School of Electrical and Power Engineering, Xuzhou, China; China University of Mining and Technology, School of Electrical and Power Engineering, Xuzhou, China; (Power Electronics and Motion Control Conference (IPEMC2020-ECCE Asia), 2020 IEEE 9th International, v.2020, 2020, pp.3443-3448)
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- 657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family
- Tekin, M; Doğ u, F; Taç yıldız, N; Akar, E; İ kincioğ ullari, A; Oğ ur, G; Yavuz, G; Babacan, E; Akar, N; ; (Clinical genetics, v.62, 2002, pp.84-88)
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