AAAAAA
Results:
1-15
|
Results: 15
Authors:
Bartsch, O
Bartlick, B
Ivell, R
Citation: O. Bartsch et al., Relaxin signalling links tyrosine phosphorylation to phosphodiesterase andadenylyl cyclase activity, MOL HUM REP, 7(9), 2001, pp. 799-809
Authors:
Einspanier, A
Muller, D
Lubberstedt, J
Bartsch, O
Jurdzinski, A
Fuhrmann, K
Ivell, R
Citation: A. Einspanier et al., Characterization of relaxin binding in the uterus of the marmoset monkey, MOL HUM REP, 7(10), 2001, pp. 963-970
Authors:
Zarreh-Hoshyari-Khah, R
Bartsch, O
Einspanier, A
Pohnke, Y
Ivell, R
Citation: R. Zarreh-hoshyari-khah et al., Bioactivity of recombinant prorelaxin from the marmoset monkey, REGUL PEPT, 97(2-3), 2001, pp. 139-146
Authors:
Zhu, G
Gillessen-Kaesbach, G
Wirth, J
Passarge, E
Bartsch, O
Citation: G. Zhu et al., Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2), AM J MED G, 98(4), 2001, pp. 317-319
Authors:
Wuyts, W
Van Hul, W
Bartsch, O
Wilkie, AOM
Meinecke, P
Citation: W. Wuyts et al., Burning down DEFECT11, AM J MED G, 100(4), 2001, pp. 331-332
Authors:
Kuhnle, U
Bartsch, O
Werner, W
Schuster, T
Citation: U. Kuhnle et al., Penoscrotal inversion, hypospadias, imperforate anus, facial anomalies, and developmental delay: definition of a new clinical syndrome, PEDIAT SURG, 16(5-6), 2000, pp. 396-399
Authors:
Talvik, I
Ounap, K
Bartsch, O
Ilus, T
Uibo, O
Talvik, T
Citation: I. Talvik et al., Boy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32 -> qter, AM J MED G, 93(5), 2000, pp. 399-402
Authors:
Bartsch, O
Wagner, A
Hinkel, GK
Krebs, P
Stumm, M
Schmalenberger, B
Bohm, S
Balci, S
Majewski, F
Citation: O. Bartsch et al., FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy, EUR J HUM G, 7(7), 1999, pp. 748-756
Authors:
Bartsch, O
Kress, W
Wagner, A
Seemanova, E
Citation: O. Bartsch et al., The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28: report of the first familial case, CYTOG C GEN, 85(3-4), 1999, pp. 310-314
Authors:
Seemanova, E
Bartsch, O
Citation: E. Seemanova et O. Bartsch, Mulibrey nanism and Wilms tumor, AM J MED G, 85(1), 1999, pp. 76-78
Authors:
Bartsch, O
Wagner, A
Hinkel, GK
Lichtner, P
Murken, J
Schuffenhauer, S
Citation: O. Bartsch et al., No evidence for chromosomal microdeletions at the second DiGeorge syndromelocus on 10p near D10S585, AM J MED G, 83(5), 1999, pp. 425-426
Authors:
Bartsch, O
Ludwig, D
Schwinger, E
Tympner, KD
Citation: O. Bartsch et al., Severe complications and gastric carcinoma in Mulvihill-Smith syndrome, J MED GENET, 36(2), 1999, pp. 175-175
Authors:
Bartsch, O
Horstmann, S
Toprak, K
Klempnauer, KH
Ferrari, S
Citation: O. Bartsch et al., Identification of cyclin A/Cdk2 phosphorylation sites in B-Myb, EUR J BIOCH, 260(2), 1999, pp. 384-391
Authors:
Ounap, K
Laidre, P
Bartsch, O
Rein, R
Lipping-Sitska, M
Citation: K. Ounap et al., Familial Williams-Beuren syndrome, AM J MED G, 80(5), 1998, pp. 491-493
Authors:
Hinkel, GK
Bartsch, O
Fischer, R
Werner, W
Citation: Gk. Hinkel et al., A supernumerary marker chromosome vertical bar dic(22)(q11)vertical bar ina family with hypoparathyroidism, sensorineural deafness and renal dysplasiav, MONATS KIND, 146(11), 1998, pp. 1034-1038
Risultati:
1-15
|