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Results:
1-7
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Results: 7
Authors:
Kramer, F
White, K
Pauleikhoff, D
Gehrig, A
Passmore, L
Rivera, A
Rudolph, G
Kellner, U
Andrassi, M
Lorenz, B
Rohrschneider, K
Blankenagel, A
Jurklies, B
Schilling, H
Schutt, F
Holz, FG
Weber, BHF
Citation: F. Kramer et al., Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration, EUR J HUM G, 8(4), 2000, pp. 286-292
Authors:
Stohr, H
Mah, N
Schulz, HL
Gehrig, A
Frohlich, S
Weber, BHF
Citation: H. Stohr et al., EST mining of the UniGene dataset to identify retina-specific genes, CYTOG C GEN, 91(1-4), 2000, pp. 267-277
Authors:
Jeanneret, C
Labs, KH
Aschwanden, M
Gehrig, A
Jager, KA
Citation: C. Jeanneret et al., Measured versus calculated venous cross sectional area., ULTRASC MED, 21(1), 2000, pp. 16-19
Authors:
Aschwanden, M
Labs, KH
Jeanneret, C
Gehrig, A
Jaeger, KA
Citation: M. Aschwanden et al., The value of rapid D-dimer testing combined with structured clinical evaluation for the diagnosis of deep vein thrombosis, J VASC SURG, 30(5), 1999, pp. 929-935
Authors:
Stohr, H
Klein, J
Gehrig, A
Koehler, MR
Jurklies, B
Kellner, U
Leo-Kottler, B
Schmid, M
Weber, BHF
Citation: H. Stohr et al., Mapping and genomic characterization of the gene encoding diacylglycerol kinase gamma (DAGK3): assessment of its role in dominant optic atrophy (OPA1), HUM GENET, 104(1), 1999, pp. 99-105
Authors:
Gehrig, A
Weber, BHF
Lorenz, B
Andrassi, M
Citation: A. Gehrig et al., First molecular evidence for a de novo mutation in RS1 (XLRS1) associated with X linked juvenile retinoschisis, J MED GENET, 36(12), 1999, pp. 932-934
Authors:
Gehrig, A
White, K
Lorenz, B
Andrassi, M
Clemens, S
Weber, BHF
Citation: A. Gehrig et al., Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis, CLIN GENET, 55(6), 1999, pp. 461-465
Risultati:
1-7
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