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Results: 1-8 |
Results: 8
High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness
Authors: Wiszniewski, W Sobieszczanska-Radoszewska, L Nowakowska-Szyrwinska, E Obersztyn, E Bal, J
Citation: W. Wiszniewski et al., High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness, GENET TEST, 5(2), 2001, pp. 147-148
Mutation in the class II trans-activator leading to a mild immunodeficiency
Authors: Wiszniewski, W Fondaneche, MC Le Deist, FO Kanariou, M Selz, FO Brousse, N Steimle, V Barbieri, G Alcaide-Loridan, C Charron, D Fischer, A Lisowska-Grospierre, B
Citation: W. Wiszniewski et al., Mutation in the class II trans-activator leading to a mild immunodeficiency, J IMMUNOL, 167(3), 2001, pp. 1787-1794
A comparative study of the on-off switching behavior of metal-insulator-metal antifuses
Authors: Li, WT McKenzie, DR Wiszniewski, W
Citation: Wt. Li et al., A comparative study of the on-off switching behavior of metal-insulator-metal antifuses, IEEE ELEC D, 21(6), 2000, pp. 295-297
Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B
Authors: Wiszniewski, W Fondaneche, MC Lambert, N Masternak, K Picard, C Notarangelo, L Schwartz, K Bal, J Reith, W Alcaide, C de saint Basile, G Fischer, A Lisowska-Grospierre, B
Citation: W. Wiszniewski et al., Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B, IMMUNOGENET, 51(4-5), 2000, pp. 261-267
Breakdown mechanism of Al2O3 based metal-to-metal antifuses
Authors: Li, WT McKenzie, DR McFall, WD Zhang, QC Wiszniewski, W
Citation: Wt. Li et al., Breakdown mechanism of Al2O3 based metal-to-metal antifuses, SOL ST ELEC, 44(9), 2000, pp. 1557-1562
In vitro expression analysis of R68G and R68S mutations in phenylalanine hydroxylase gene
Authors: Zekanowski, C Perez, B Desviat, LR Wiszniewski, W Ugarte, M
Citation: C. Zekanowski et al., In vitro expression analysis of R68G and R68S mutations in phenylalanine hydroxylase gene, ACT BIOCH P, 47(2), 2000, pp. 365-369
Refined genetic and physical localization of the Wagner disease (WGN1) locus and the genes CRTL1 and CSPG2 to a 2- to 2.5-cM region of chromosome 5q14.3
Authors: Perveen, R Hart-Holden, N Dixon, MJ Wiszniewski, W Fryer, AE Brunner, HG Pinkners, AJLH van Beersum, SEC Black, GCM
Citation: R. Perveen et al., Refined genetic and physical localization of the Wagner disease (WGN1) locus and the genes CRTL1 and CSPG2 to a 2- to 2.5-cM region of chromosome 5q14.3, GENOMICS, 57(2), 1999, pp. 219-226
A novel hereditary developmental vitreoretinopathy with multiple ocular abnormalities localizing to a 5-cM region of chromosome 5q13-q14
Authors: Black, GCM Perveen, R Wiszniewski, W Dodd, CL Donnai, D McLeod, D
Citation: Gcm. Black et al., A novel hereditary developmental vitreoretinopathy with multiple ocular abnormalities localizing to a 5-cM region of chromosome 5q13-q14, OPHTHALMOL, 106(11), 1999, pp. 2074-2081
Risultati: 1-8 |