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Results:
1-8
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Results: 8
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:
Oldenburg, J
Ivaskevicius, V
Rost, S
Fregin, A
White, K
Holinski-Feder, E
Muller, CR
Weber, BHF
Citation: J. Oldenburg et al., Evaluation of DHPLC in the analysis of hemophilia A, J BIOCH BIO, 47(1-2), 2001, pp. 39-51
Authors:
Pfeifer, D
Poulat, F
Holinski-Feder, E
Kooy, F
Scherer, G
Citation: D. Pfeifer et al., The SOX8 gene is located within 700 kb of the tip of chromosome 16p and isdeleted in a patient with ATR-16 syndrome, GENOMICS, 63(1), 2000, pp. 108-116
Authors:
Rost, I
Duroux, A
Toniolo, D
Holinski-Feder, E
Kozlik-Feldmann, R
Citation: I. Rost et al., Barth syndrome: X-linked dilated cardiomyopathy, MONATS KIND, 148(3), 2000, pp. 246-250
Authors:
Holinski-Feder, E
Reyniers, E
Uhrig, S
Golla, A
Wauters, J
Kroisel, P
Bossuyt, P
Rost, I
Jedele, K
Zierler, H
Schwab, S
Wildenauer, D
Speicher, MR
Willems, PJ
Meitinger, T
Kooy, RF
Citation: E. Holinski-feder et al., Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3), AM J HU GEN, 66(1), 2000, pp. 16-25
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
DNA analysis of Huntington's disease - Five years of experience in Germany, Austria, and Switzerland
Authors:
Laccone, F
Engel, U
Holinski-Feder, E
Weigell-Weber, M
Marczinek, K
Nolte, D
Morris-Rosendahl, DJ
Zuhlke, C
Fuchs, K
Weirich-Schwaiger, H
Schluter, G
von Beust, G
Vieira-Saecker, AMM
Weber, BHF
Riess, O
Citation: F. Laccone et al., DNA analysis of Huntington's disease - Five years of experience in Germany, Austria, and Switzerland, NEUROLOGY, 53(4), 1999, pp. 801-806
Authors:
Klopstock, T
Chahrokh-Zadeh, S
Holinski-Feder, E
Meindl, A
Gasser, T
Pongratz, D
Muller-Felber, W
Citation: T. Klopstock et al., Markedly different course of Friedreich's ataxia in sib pairs with similarGAA repeat expansions in the frataxin gene, ACT NEUROP, 97(2), 1999, pp. 139-142
Risultati:
1-8
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