Genetic fever--Internet consultation, mutation in the envelope
Korppi, M.; Korhonen, J.; Lindström, K.; Mononen, T.
Duodecim; Laaketieteellinen Aikakauskirja 119(16): 1567-1571
2003
ISSN/ISBN: 0012-7183 PMID: 14535030 Document Number: 554520
Document emailed within 1 workday
Related Documents
Xu, Q.; Zhang, X.; Jing, J.; Shi, B.; Wang, S.; Zhou, B.; Chen, P. 2015: Hsp70 Fused with the Envelope Glycoprotein E0 of Classical Swine Fever Virus Enhances Immune Responses in Balb/c Mice Bing du Xue Bao 31(4): 363-369Zhang, H.; Tully, D.C.; Hoffmann, F.G.; He, J.; Kankasa, C.; Wood, C. 2010: Restricted genetic diversity of HIV-1 subtype C envelope glycoprotein from perinatally infected Zambian infants Plos one 5(2): E9294
Kumar, S.; Prakash, N.; Agarwal, K.N. 1979: Cyclic AMP control of the envelope growth in Escherichia coli: envelope morphology of the mutants in cya and crp genes Indian Journal of Experimental Biology 17(4): 325-327
Freund, M.M.; Basteyns, E.; Martin, N.; De Meyer, R. 1975: Genetic examination of patients in consultation for sterility or miscarrigae Journal de Genetique Humaine 23 Suppl: 112-113
Nazarenko, L.P.; Nazarenko, S.A.; Puzyrev, V.P. 1986: Case of medical-genetic consultation for Fanconi's anemia Pediatriia 1986(12): 49-50
Pettersson, T.; Karenko, L.; Ranki, A. 1999: Mutation of the cytokine receptor behind periodical fever syndrome Duodecim; Laaketieteellinen Aikakauskirja 115(18): 1951-1953
Durnov, L.A.; Sotnikova, E.N. 1985: Deontological aspects of medical genetic consultation in pediatric oncology Pediatriia 1985(8): 67-69
Landau, Y.; Vinker, S.; Shani, M.; Nakar, S. 2008: Has the time come to adopt consultation time as a new technology for "the basket"? A literature review of the relations between consultation duration and consultation quality in primary care Harefuah 147(12): 1016-20 1026
Krenová, D.; Jirsová, Z.; Housa, D.; Liska, F.; Soltysová, L.; Kaspárek, R.; Bílá, V.; Pravenec, M.; Kren, V. 1999: Genetic analysis of the rat hypodactylous mutation Folia Biologica 45(3): 81-86
Matsuo, M.; Urano, M.; Saito, K. 2009: Gene mutation and genetic counseling Nihon Rinsho. Japanese Journal of Clinical Medicine 67(6): 1191-1196
Danielov, M.B.; Utin, A.V. 1985: Medico-genetic consultation of families of oligophrenic patients (according to empirical risk findings) Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 85(3): 394-398
Malik, M.R.; El Bushra, H.E.; Opoka, M.; Formenty, P.; Velayudhan, R.; Eremin, S. 2013: Strategic approach to control of viral haemorrhagic fever outbreaks in the Eastern Mediterranean Region: report from a regional consultation Eastern Mediterranean Health Journal 19(10): 892-897
Samuel, I.; Tomas, E.; Portocală 1976: Interaction between ceruloplasmin and Sendai virus envelope components. Note i. Gel-filtration of Tween 20-solubilized envelope components Virologie 27(2): 119-125
Zatsepina, O.V.; Polyakov VYu; Chentsov YuS 1982: Nuclear envelope formation around metaphase chromosomes: chromosome decondensation and nuclear envelope reconstitution during mitosis European Journal of Cell Biology 26(2): 277-283
Ocran, K.; Schmidt, H.H. 2000: Value of genetic diagnosis of C282Y mutation in patients with hereditary hemochromatosis Zeitschrift für Gastroenterologie 38(2): 205-207
Dutcher, S.K.; Gibbons, W.; Inwood, W.B. 1988: A genetic analysis of suppressors of the PF10 mutation in Chlamydomonas reinhardtii Genetics 120(4): 965-976
Berg, R.L.; Kryshova, N.A.; Ozeretskovskaia, N.G.; Artemchuk, N.L.; Begzhanov, K.B. 1973: Population-genetic approach to studying the mutation process using 4 forms of myopathy as an example Genetika 9(10): 127-138
Kosztolányi, G. 2001: Clinical and genetic consequences of ring chromosome, a structural genome mutation Orvosi Hetilap 142(8): 379-381
Hidaka, K.; Iuchi, I.; Yamasaki, T.; Ohhara, M.; Shoda, T.; Primo-Parmo, S.; Ladu, B.N. 1992: Identification of two different genetic mutation associated with silent phenotypes for human serum cholinesterase in Japanese Rinsho Byori. Japanese Journal of Clinical Pathology 40(5): 535-540
Shem-Tov, N.; Shohat, M. 1994: Amplification of trinucleotide repeats--a new mutation mechanism causing common genetic diseases Harefuah 127(7-8): 268-273