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Results:
1-10
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Results: 10
Authors:
Langer, S
Fauth, C
Rocchi, M
Murken, J
Speicher, MR
Citation: S. Langer et al., AcroM fluorescent in situ hybridization analyses of marker chromosomes, HUM GENET, 109(2), 2001, pp. 152-158
Authors:
Holinski-Feder, E
Muller-Koch, Y
Friedl, W
Moselein, G
Keller, G
Plaschke, J
Ballhausen, W
Gross, M
Baldwin-Jedele, K
Jungck, M
Mangold, E
Vogelsang, H
Schackert, HK
Lohse, P
Murken, J
Meitinger, T
Citation: E. Holinski-feder et al., DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2, J BIOCH BIO, 47(1-2), 2001, pp. 21-32
Authors:
Schmidt, H
Uhrig, S
Lederer, G
Murken, J
Speicher, MR
Schuffenhauer, S
Citation: H. Schmidt et al., Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito andasymmetry, J MED GENET, 37(10), 2000, pp. 804-806
Authors:
Kolbe, M
Murken, J
Pistolek, D
Eggeler, G
Klam, HJ
Citation: M. Kolbe et al., Direct assessment of the creep strength of DS cast turbine blades using miniature creep specimens, MATER WERKS, 30(8), 1999, pp. 465-472
Authors:
Holinski-Feder, E
Chahrockh-Zadeh, S
Rittinger, O
Jedele, KB
Gasteiger, M
Lenski, C
Murken, J
Golla, A
Citation: E. Holinski-feder et al., Nonsyndromic X-linked mental retardation: Mapping of MRX58 to the pericentromeric region, AM J MED G, 86(2), 1999, pp. 102-106
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:
Schuffenhauer, S
Leifheit, HJ
Lichtner, P
Peters, H
Murken, J
Emmerich, P
Citation: S. Schuffenhauer et al., De novo deletion (14)(q11.2q13) including PAX9: clinical and molecular findings, J MED GENET, 36(3), 1999, pp. 233-236
Authors:
Brand, S
Strom, TM
Weber, MM
Schuffenhauer, S
Murken, J
Engelhardt, D
Citation: S. Brand et al., Primary hypogonadism with chromosome constellation of true hermaphroditismand XX maleness, INTERNIST, 40(4), 1999, pp. 437-441
Authors:
Murken, J
Citation: J. Murken, Ethical problems in the context of genetic counseling and diagnostics, INTERNIST, 40(3), 1999, pp. 286-293
Authors:
Uhrig, S
Schuffenhauer, S
Fauth, C
Wirtz, A
Daumer-Haas, C
Apacik, C
Cohen, M
Muller-Navia, J
Cremer, T
Murken, J
Speicher, MR
Citation: S. Uhrig et al., Multiplex-FISH for pre- and postnatal diagnostic applications, AM J HU GEN, 65(2), 1999, pp. 448-462
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