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Results:
1-20
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Results: 20
Authors:
Schurmann, M
Reichel, P
Muller-Myhsok, B
Schlaak, M
Muller-Quernheim, J
Schwinger, E
Citation: M. Schurmann et al., Results from a genome-wide search for predisposing genes in sarcoidosis, AM J R CRIT, 164(5), 2001, pp. 840-846
Authors:
Zimprich, A
Grabowski, M
Asmus, F
Naumann, M
Berg, D
Bertram, M
Scheidtmann, K
Kern, P
Winkelmann, F
Muller-Myhsok, B
Riedel, L
Bauer, M
Muller, T
Castro, M
Meitinger, T
Strom, TM
Gasser, T
Citation: A. Zimprich et al., Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome, NAT GENET, 29(1), 2001, pp. 66-69
Authors:
West, AB
Zimprich, A
Lockhart, PJ
Farrer, M
Singleton, A
Holtom, B
Lincoln, S
Hofer, A
Hill, L
Muller-Myhsok, B
Wszolek, ZK
Hardy, J
Gasser, T
Citation: Ab. West et al., Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes, EUR J HUM G, 9(9), 2001, pp. 659-666
Authors:
Schurmann, M
Reichel, P
Muller-Myhsok, B
Dieringer, T
Wurm, K
Schlaak, M
Muller-Quernheim, J
Schwinger, E
Citation: M. Schurmann et al., Angiotensin-converting enzyme (ACE) gene polymorphisms and familial occurrence of sarcoidosis, J INTERN M, 249(1), 2001, pp. 77-83
Authors:
Asmus, F
Zimprich, A
Naumann, M
Berg, D
Bertram, M
Ceballos-Baumann, A
Pruszak-Seel, R
Kabus, C
Dichgans, M
Fuchs, S
Muller-Myhsok, B
Gasser, T
Citation: F. Asmus et al., Inherited myoclonus-dystonia syndrome: Narrowing the 7q21-q31 locus in German families, ANN NEUROL, 49(1), 2001, pp. 121-124
Authors:
Schurmann, M
Lympany, PA
Reichel, P
Muller-Myhsok, B
Wurm, K
Schlaak, M
Muller-Quernheim, J
du Bois, RM
Schwinger, E
Citation: M. Schurmann et al., Familiar sarcoidosis is linked to the major histocompatibility complex region, AM J R CRIT, 162(3), 2000, pp. 861-864
Authors:
Busjahn, A
Knoblauch, H
Faulhaber, HD
Aydin, A
Uhlmann, R
Tuomilehto, J
Kaprio, J
Jedrusik, P
Januszewicz, A
Strelau, J
Schuster, H
Luft, FC
Muller-Myhsok, B
Citation: A. Busjahn et al., A region on chromosome 3 is linked to dizygotic twinning, NAT GENET, 26(4), 2000, pp. 398-399
Authors:
Agrawal, S
Gupta, A
Yachha, SK
Muller-Myhsok, B
Mehrotra, P
Agarwal, SS
Citation: S. Agrawal et al., Association of human leucocyte-DR and DQ antigens in coeliac disease: A family study, J GASTR HEP, 15(7), 2000, pp. 771-774
Authors:
Schlotmann, T
Waase, I
Julch, C
Klauenberg, U
Muller-Myhsok, B
Dietrich, M
Fleischer, B
Broker, BM
Citation: T. Schlotmann et al., CD4 alpha beta T lymphocytes express high levels of the T lymphocyte antigen CTLA-4 (CD152) in acute malaria, J INFEC DIS, 182(1), 2000, pp. 367-370
Authors:
Pei, WD
Baron, H
Muller-Myhsok, B
Knoblauch, H
Al-Yahyaee, SA
Hui, RT
Wu, XG
Liu, LS
Busjahn, A
Luft, FC
Schuster, H
Citation: Wd. Pei et al., Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families, CLIN GENET, 57(1), 2000, pp. 29-34
Authors:
Knoblauch, H
Muller-Myhsok, B
Busjahn, A
Ben Avi, L
Bahring, S
Baron, H
Heath, SC
Uhlmann, R
Faulhaber, HD
Shpitzen, S
Aydin, A
Reshef, A
Rosenthal, M
Eliav, O
Muhl, A
Lowe, A
Schurr, D
Harats, D
Jeschke, E
Friedlander, Y
Schuster, H
Luft, FC
Leitersdorf, E
Citation: H. Knoblauch et al., A cholesterol-lowering gene maps to chromosome 13q, AM J HU GEN, 66(1), 2000, pp. 157-166
Authors:
Knoblauch, H
Busjahn, A
Muller-Myhsok, B
Faulhaber, HD
Schuster, H
Uhlmann, R
Luft, FC
Citation: H. Knoblauch et al., Peroxisome proliferator-activated receptor gamma gene locus is related to body mass index and lipid values in healthy nonobese subjects, ART THROM V, 19(12), 1999, pp. 2940-2944
Authors:
Nagy, Z
Busjahn, A
Bahring, S
Faulhaber, HD
Gohlke, HR
Knoblauch, H
Rosenthal, M
Muller-Myhsok, B
Schuster, K
Luft, FC
Citation: Z. Nagy et al., Quantitative trait loci for blood pressure exist near the IGF-1, the Liddle syndrome, the angiotensin II-receptor gene and the renin loci in man, J AM S NEPH, 10(8), 1999, pp. 1709-1716
Authors:
Muller-Myhsok, B
Grimm, T
Citation: B. Muller-myhsok et T. Grimm, Linkage analysis and genetic models in dyslexia - considerations pertaining to discrete trait analysis and quantitative trait analyses, EUR CHILD A, 8, 1999, pp. 40-42
Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15
Authors:
Nothen, MM
Schulte-Korne, G
Grimm, T
Cichon, S
Vogt, IR
Muller-Myhsok, B
Propping, P
Remschmidt, H
Citation: Mm. Nothen et al., Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15, EUR CHILD A, 8, 1999, pp. 56-59
Authors:
Ziegler, A
Hebebrand, J
Kastner, C
Muller-Myhsok, B
Citation: A. Ziegler et al., Significant evidence for linkage of a simulated trait to D1G024-A conclusion reached using multiallelic transmission/disequilibrium tests, GENET EPID, 17, 1999, pp. S785-S789
Authors:
Arolt, V
Lencer, R
Purmann, S
Schurmann, M
Muller-Myhsok, B
Krecker, K
Schwinger, E
Citation: V. Arolt et al., Testing for linkage of eye tracking dysfunction and schizophrenia to markers an chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia, AM J MED G, 88(6), 1999, pp. 603-606
Authors:
Boeckel, T
Dierks, A
Vergopoulos, A
Bahring, S
Knoblauch, H
Muller-Myhsok, B
Baron, H
Aydin, A
Bein, G
Luft, FC
Schuster, H
Citation: T. Boeckel et al., A new mutation in the elastin gene causing supravalvular aortic stenosis, AM J CARD, 83(7), 1999, pp. 1141
Authors:
Zuhlke, C
Gehlken, U
Purmann, S
Kunisch, M
Muller-Myhsok, B
Kreuz, F
Laccone, F
Citation: C. Zuhlke et al., Linkage disequilibrium and haplotype analysis in German Friedreich ataxia families, HUMAN HERED, 49(2), 1999, pp. 90-96
Authors:
Hoerauf, A
Hammer, S
Muller-Myhsok, B
Rupprecht, H
Citation: A. Hoerauf et al., Intra-abdominal Candida infection during acute necrotizing pancreatitis has a high prevalence and is associated with increased mortality, CRIT CARE M, 26(12), 1998, pp. 2010-2015
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1-20
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