AAAAAA
Results:
1-15
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Results: 15
Authors:
Kitsos, G
Eiberg, H
Economou-Petersen, E
Wirtz, MK
Kramer, PL
Aspiotis, M
Tommerup, N
Petersen, MB
Psilas, K
Citation: G. Kitsos et al., Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree, EUR J HUM G, 9(6), 2001, pp. 452-457
Authors:
Thiselton, DL
Alexander, C
Morris, A
Brooks, S
Rosenberg, T
Eiberg, H
Kjer, B
Kjer, P
Bhattacharya, SS
Votruba, M
Citation: Dl. Thiselton et al., A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect, HUM GENET, 109(5), 2001, pp. 498-502
Authors:
Eiberg, H
Shaumburg, HL
Von Gontard, A
Rittig, S
Citation: H. Eiberg et al., Linkage study of a large Danish 4-generation family with urge incontinenceand nocturnal enuresis, J UROL, 166(6), 2001, pp. 2401-2403
Authors:
von Gontard, A
Schaumburg, H
Hollmann, E
Eiberg, H
Rittig, S
Citation: A. Von Gontard et al., The genetics of enuresis: A review, J UROL, 166(6), 2001, pp. 2438-2443
Authors:
Klomp, LWJ
Bull, LN
Knisely, AS
van der Doelen, MAM
Juijn, JA
Berger, R
Forget, S
Nielsen, IM
Eiberg, H
Houwen, RHJ
Citation: Lwj. Klomp et al., A missense mutation in FIC1 is associated with Greenland familial cholestasis, HEPATOLOGY, 32(6), 2000, pp. 1337-1341
Authors:
Hansen, L
Urioste, S
Petersen, HV
Jensen, JN
Eiberg, H
Barbetti, F
Serup, P
Hansen, T
Pedersen, O
Citation: L. Hansen et al., Missense mutations in the human insulin promoter factor-1 gene and their relation to maturity-onset diabetes of the young and late-onset type 2 diabetes mellitus in Caucasians, J CLIN END, 85(3), 2000, pp. 1323-1326
Authors:
Hansen, L
Jensen, JN
Urioste, S
Petersen, HV
Pociot, F
Eiberg, H
Kristiansen, OP
Hansen, T
Serup, P
Nerup, J
Pedersen, O
Citation: L. Hansen et al., NeuroD/BETA2 gene variability and diabetes - No associations to late-onsettype 2 diabetes but an A45 allele may represent a susceptibility marker for type 1 diabetes among Danes, DIABETES, 49(5), 2000, pp. 876-878
Authors:
Bross, P
Pedersen, P
Winter, V
Nyholm, M
Johansen, BN
Olsen, RKJ
Corydon, MJ
Andresen, BS
Eiberg, H
Kolvraa, S
Gregersen, N
Citation: P. Bross et al., A polymorphic variant in the human electron transfer flavoprotein alpha-chain (alpha-T171) displays decreased thermal stability and is overrepresented in very-long-chain acyl-CoA dehydrogenase-deficient patients with mild childhood presentation, MOL GEN MET, 67(2), 1999, pp. 138-147
Authors:
Behrends, S
Kazmierczak, B
Steenpass, A
Knauf, B
Bullerdiek, J
Scholz, H
Eiberg, H
Citation: S. Behrends et al., Assignment of GUCY1B2, the gene coding for the beta(2) subunit of human guanylyl cyclase to chromosomal band 13q14.3 between markers D13S168 and D13S155, GENOMICS, 55(1), 1999, pp. 126-127
Authors:
von Gontard, A
Eiberg, H
Hollmann, E
Rittig, S
Lehmkuhl, G
Citation: A. Von Gontard et al., Molecular genetics of nocturnal enuresis: Linkage to a locus on chromosome22, SC J UROL N, 33, 1999, pp. 76-80
Authors:
Sorensen, CB
Ladekjaer-Mikkelsen, AS
Andresen, BS
Brandrup, F
Veien, NK
Buus, SK
Anton-Lamprecht, I
Kruse, TA
Jensen, PKA
Eiberg, H
Bolund, L
Gregersen, N
Citation: Cb. Sorensen et al., Identification of novel and known mutations in the genes for keratin 5 and14 in Danish patients with epidermolysis bullosa simplex: Correlation between genotype and phenotype, J INVES DER, 112(2), 1999, pp. 184-190
Authors:
Moller, AM
Ek, J
Durviaux, SM
Urhammer, SA
Clausen, JO
Eiberg, H
Hansen, T
Rousseau, GG
Lemaigre, FP
Pedersen, O
Citation: Am. Moller et al., Hepatocyte nuclear factor-6: associations between genetic variability and Type II diabetes and between genetic variability and estimates of insulin secretion, DIABETOLOG, 42(8), 1999, pp. 1011-1016
Authors:
Dalgaard, LT
Hansen, T
Urhammer, SA
Clausen, JO
Eiberg, H
Pedersen, O
Citation: Lt. Dalgaard et al., Intermediate expansions of a GAA repeat in the frataxin gene are not associated with type 2 diabetes or altered glucose-induced beta-cell function inDanish Caucasians, DIABETES, 48(4), 1999, pp. 914-917
Authors:
Koefoed, P
Hasholt, L
Fenger, K
Nielsen, JE
Eiberg, H
Buschard, K
Sorensen, SA
Citation: P. Koefoed et al., Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1, HUM GENET, 103(5), 1998, pp. 564-569
Authors:
Urhammer, SA
Hansen, T
Ekstrom, CT
Eiberg, H
Pedersen, O
Citation: Sa. Urhammer et al., The Ala/Val98 polymorphism of the hepatocyte nuclear factor-1 alpha gene contributes to the interindividual variation in serum C-peptide response during an oral glucose tolerance test: Evidence from studies of 231 glucose-tolerant first degree relatives of type 2 diabetic probands, J CLIN END, 83(12), 1998, pp. 4506-4509
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