AAAAAA

   
Results: 1-8 |
Results: 8

Authors: Gianfrancesco, F Sanges, R Esposito, T Tempesta, S Rao, E Rappold, G Archidiacono, N Graves, JAM Forabosco, A D'Urso, M
Citation: F. Gianfrancesco et al., Differential divergence of three human pseudoautosomal genes and their mouse homologs: Implications for sex chromosome evolution, GENOME RES, 11(12), 2001, pp. 2095-2100

Authors: Ogata, T Onigata, K Hotsubo, T Matsuo, N Rappold, G
Citation: T. Ogata et al., Growth hormone and gonadotropin-releasing hormone analog therapy in haploinsufficiency of SHOX, ENDOCR J, 48(3), 2001, pp. 317-322

Authors: Ogata, T Wakui, K Kosho, T Muroya, K Yamanouchi, Y Takano, T Fukushima, Y Rappold, G Suzuki, Y
Citation: T. Ogata et al., Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation, AM J MED G, 92(4), 2000, pp. 256-259

Authors: Oner, G Jauch, A Eggermann, T Hardwick, R Kirsch, S Schiebel, K Rappold, G Robson, L Smith, A
Citation: G. Oner et al., Mosaic rearrangement of chromosome 18: Characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin, AM J MED G, 92(2), 2000, pp. 101-106

Authors: Lien, S Szyda, J Schechinger, B Rappold, G Arnheim, N
Citation: S. Lien et al., Evidence for heterogeneity in recombination in the human pseudoautosomal region: High resolution analysis by sperm typing and radiation-hybrid mapping, AM J HU GEN, 66(2), 2000, pp. 557-566

Authors: Bottner, M Laaff, M Schechinger, B Rappold, G Unsicker, K Suter-Crazzolara, C
Citation: M. Bottner et al., Characterization of the rat, mouse, and human genes of growth/differentiation factor-15/macrophage inhibiting cytokine-1 (GDF-15/MIC-1), GENE, 237(1), 1999, pp. 105-111

Authors: Hess, M Goldammer, T Gelhaus, A Ried, K Rappold, G Eggen, A Bishop, MD Schwerin, M Horstmann, RD
Citation: M. Hess et al., Physical assignment of the bovine MHC class IIa and class IIb genes, CYTOG C GEN, 85(3-4), 1999, pp. 244-247

Authors: Spranger, S Schiller, S Jauch, A Wolff, K Rauterberg-Ruland, I Hager, D Tariverdian, G Troger, J Rappold, G
Citation: S. Spranger et al., Leri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3, AM J MED G, 83(5), 1999, pp. 367-371
Risultati: 1-8 |