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Results: 5

Authors: Gronskov, K Olsen, JH Sand, A Pedersen, W Carlsen, N Jylling, AMB Lyngbye, T Brondum-Nielsen, K Rosenberg, T
Citation: K. Gronskov et al., Population-based risk estimates of Wilms tumor in sporadic aniridia - A comprehensive mutation screening procedure of PAX6 identifies 80% of mutations in aniridia, HUM GENET, 109(1), 2001, pp. 11-18

Authors: Antoniadi, T Gronskov, K Sand, A Pampanos, A Brondum-Nielsen, K Petersen, MB
Citation: T. Antoniadi et al., Mutation analysis of the GJB2 (Connexin 26) gene by DGGE in Greek patientswith sensorineural deafness, HUM MUTAT, 16(1), 2000, pp. 7-12

Authors: Larsen, LA Armstrong, JSM Gronskov, K Hjalgrim, H Macpherson, JN Brondum-Nielsen, K Hasholt, L Norgaard-Pedersen, B Vuust, J
Citation: La. Larsen et al., Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles, AM J MED G, 93(2), 2000, pp. 99-106

Authors: Larsen, LA Armstrong, JSM Gronskov, K Hjalgrim, H Brondum-Nielsen, K Hasholt, L Norgaard-Pedersen, B Vuust, J
Citation: La. Larsen et al., Analysis of FMR1 (CGG)(n) alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia, EUR J HUM G, 7(7), 1999, pp. 771-777

Authors: Gronskov, K Rosenberg, T Sand, A Brondum-Nielsen, K
Citation: K. Gronskov et al., Mutational analysis of PAX6: 16 novel mutations including 5 missense mutations with a mild aniridia phenotype, EUR J HUM G, 7(3), 1999, pp. 274-286
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