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Results:
1-7
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Results: 7
Authors:
Friedl, W
Caspari, R
Uhlhaas, S
Lamberti, C
Jungck, M
Kadmon, M
Wolf, M
Fahnenstich, J
Gebert, J
Moslein, G
Mangold, E
Propping, P
Citation: W. Friedl et al., Can APC: mutation analysis contribute to therapeutic decisions in familialadenomatous polyposis? Experience from 680 FAP families, GUT, 48(4), 2001, pp. 515-521
Authors:
Kornak, U
Schulz, A
Friedrich, W
Uhlhaas, S
Kremens, B
Voit, T
Hasan, C
Bode, U
Jentsch, TJ
Kubisch, C
Citation: U. Kornak et al., Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis, HUM MOL GEN, 9(13), 2000, pp. 2059-2063
Authors:
Caspari, R
Uhlhaas, S
Friedl, W
Knapp, M
Propping, P
Citation: R. Caspari et al., Mapping of a gene for nonspecific X-linked mental retardation (MRX 75) to Xq24-q26, AM J MED G, 93(4), 2000, pp. 290-293
Authors:
Propping, P
Friedl, W
Wienker, TF
Uhlhaas, S
Zerres, K
Citation: P. Propping et al., ADULT syndrome allelic to limb mammary syndrome (LMS)?, AM J MED G, 90(2), 2000, pp. 179-182
Authors:
Trost, D
Wiebe, W
Uhlhaas, S
Schwindt, P
Schwanitz, G
Citation: D. Trost et al., Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2, J MED GENET, 37(6), 2000, pp. 452-454
Authors:
Friedl, W
Kruse, R
Uhlhaas, S
Stolte, M
Schartmann, B
Keller, KM
Jungck, M
Stern, M
Loff, S
Back, W
Propping, P
Jenne, DE
Citation: W. Friedl et al., Frequent 4-bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patients, GENE CHROM, 25(4), 1999, pp. 403-406
Authors:
Maringa, M
Uhlhaas, S
Kreyer, E
Friedl, W
Propping, P
Schmutzler, RK
Citation: M. Maringa et al., Large deletions in the BRCA1 gene are not common in a set of familial German breast cancer patients, DIS MARKER, 15(1-3), 1999, pp. 95-95
Risultati:
1-7
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