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Results:
1-13
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Results: 13
Authors:
Jacobi, FK
Meyer, J
Pusch, CM
Wissinger, B
Citation: Fk. Jacobi et al., Quantitation of heteroplasmy in mitochondrial DNA mutations by primer extension using Vent(R)(R)(exo-) DNA polymerase and RFLP analysis, MUT RES-F M, 478(1-2), 2001, pp. 141-151
Authors:
Pesch, K
Tomiuk, J
Broghammer, M
Zrenner, E
Apfelstedt-Sylla, E
Jacobi, FK
Wissinger, B
Pusch, CM
Citation: K. Pesch et al., Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders, INT J MOL M, 8(1), 2001, pp. 53-58
Authors:
Pusch, CM
Maurer, J
Ramser, J
Tomiuk, J
Achatz, H
Pesch, K
Lichtner, P
Apfelstedt-Sylla, E
Jacobi, FK
Berger, W
Meindl, A
Wissinger, B
Citation: Cm. Pusch et al., Complete form of X-linked congenital stationary night blindness: Refined mapping and evidence of genetic homogeneity, INT J MOL M, 7(2), 2001, pp. 155-161
Authors:
Jacobi, FK
Leo-Kottler, B
Mittelviefhaus, K
Zrenner, E
Meyer, J
Pusch, CM
Wissinger, B
Citation: Fk. Jacobi et al., Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy, INV OPHTH V, 42(6), 2001, pp. 1208-1214
Authors:
Scholl, HPN
Langrova, H
Pusch, CM
Wissinger, B
Zrenner, E
Apfelstedt-Sylla, E
Citation: Hpn. Scholl et al., Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene, INV OPHTH V, 42(11), 2001, pp. 2728-2736
Authors:
Czarnetzki, A
Gaudzinski, S
Pusch, CM
Citation: A. Czarnetzki et al., Hominid skull fragments from Late Pleistocene layers in Leine Valley (Sarstedt, District of Hildesheim, Germany), J HUM EVOL, 41(2), 2001, pp. 133-140
Authors:
Pusch, CM
Zeitz, C
Brandau, O
Pesch, K
Achatz, H
Feil, S
Scharfe, C
Maurer, J
Jacobi, FK
Pinckers, A
Andreasson, S
Hardcastle, A
Wissinger, B
Berger, W
Meindl, A
Citation: Cm. Pusch et al., The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein, NAT GENET, 26(3), 2000, pp. 324-327
Authors:
Jacobi, FK
Broghammer, M
Pesch, K
Zrenner, E
Berger, W
Meindl, A
Pusch, CM
Citation: Fk. Jacobi et al., Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1, HUM GENET, 107(1), 2000, pp. 89-91
Authors:
Bachmann, L
Scholz, M
Broghammer, M
Giddings, I
Pusch, CM
Citation: L. Bachmann et al., Voltage-induced release of nucleic acids from palaeontological samples, ELECTROPHOR, 21(8), 2000, pp. 1488-1492
Authors:
Pusch, CM
Bachmann, L
Broghammer, M
Scholz, M
Citation: Cm. Pusch et al., Internal Alu-polymerase chain reaction: A sensitive contamination monitoring protocol for DNA extracted from prehistoric animal bones, ANALYT BIOC, 284(2), 2000, pp. 408-411
Authors:
Pusch, CM
Nicholson, GJ
Bachmann, L
Scholz, M
Citation: Cm. Pusch et al., Degenerate oligonucleotide-primed preamplification of ancient DNA allows the retrieval of authentic DNA sequences, ANALYT BIOC, 279(1), 2000, pp. 118-122
Authors:
Scholz, M
Bachmann, L
Nicholson, GJ
Bachmann, J
Giddings, I
Ruschoff-Thale, B
Czarnetzki, A
Pusch, CM
Citation: M. Scholz et al., Genomic differentiation of neanderthals and anatomically modern man allowsa fossil-DNA-based classification of morphologically indistinguishable hominid bones, AM J HU GEN, 66(6), 2000, pp. 1927-1932
Authors:
Scholz, M
Carreno, LT
Pusch, CM
Citation: M. Scholz et al., Modified application of dot blot analysis to the determination of fossil Os parietale from Warendorf-Neuwarendorf, ANTHROPOLOG, 103(2), 1999, pp. 307-311
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