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Results: 22
Authors:
Cai, L
Lumsden, A
Guenther, UP
Neldner, SA
Zach, S
Knoblauch, H
Ramesar, R
Hohl, D
Callen, DF
Neldner, KH
Lindpaintner, K
Richards, RI
Struk, B
Citation: L. Cai et al., A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthomaelasticum, J MOL MED-J, 79(9), 2001, pp. 536-546
Authors:
Knoblauch, H
Citation: H. Knoblauch, The gospel of television - A cultural study of the life-affirming religionof the media, KOLNER Z SO, 53(2), 2001, pp. 350-355
Authors:
Knoblauch, H
Citation: H. Knoblauch, Religion and relations between the sexes, KOLNER Z SO, 53(2), 2001, pp. 350-355
Authors:
Knoblauch, H
Citation: H. Knoblauch, Religion and identity - Experiencing pluralism, KOLNER Z SO, 53(2), 2001, pp. 350-355
Authors:
Knoblauch, H
Citation: H. Knoblauch, The religious field - The economics of salvation, KOLNER Z SO, 53(2), 2001, pp. 350-355
Authors:
Knoblauch, H
Citation: H. Knoblauch, Transformations of religion and church in East Germany, 1989-1999, KOLNER Z SO, 53(2), 2001, pp. 350-355
Authors:
Knoblauch, H
Citation: H. Knoblauch, Intensive experiences of young people - Qualitaive-empirical access and religious-pedagogical relevance, KOLNER Z SO, 53(2), 2001, pp. 350-355
Authors:
Knoblauch, H
Citation: H. Knoblauch, Religion as a chain of memory, J RELIG, 81(3), 2001, pp. 527-528
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:
Schiller, S
Spranger, S
Schechinger, B
Fukami, M
Merker, S
Drop, SLS
Troger, J
Knoblauch, H
Kunze, J
Seidel, J
Rappold, GA
Citation: S. Schiller et al., Phenotypic variation and genetic heterogeneity in Leri-Weill syndrome, EUR J HUM G, 8(1), 2000, pp. 54-62
Authors:
Knoblauch, H
Schuster, H
Luft, JC
Reich, J
Citation: H. Knoblauch et al., A pathway model of lipid metabolism to predict the effect of genetic variability on lipid levels, J MOL MED-J, 78(9), 2000, pp. 507-515
Authors:
Woywodt, A
Knoblauch, H
Kettritz, R
Schneider, W
Gobel, U
Citation: A. Woywodt et al., Sudden death and Wegener's granulomatosis of the pituitary, SC J RHEUM, 29(4), 2000, pp. 264-266
Authors:
Knoblauch, H
Thiel, G
Tinschert, S
Korner, H
Tennstedt, C
Chaoui, R
Kohlhase, J
Dixkens, C
Blanck, C
Citation: H. Knoblauch et al., Clinical and molecular cytogenetic studies of a large de novo interstitialdeletion 16q11.2-16q21 including the putative transcription factor gene SALL1, J MED GENET, 37(5), 2000, pp. 389-392
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:
Heath, C
Knoblauch, H
Luff, P
Citation: C. Heath et al., Technology and social interaction: the emergence of 'workplace studies', BR J SOCIOL, 51(2), 2000, pp. 299-320
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
Linkage but lack of association for blood pressure and the alpha-adducin locus in normotensive twins
Authors:
Busjahn, A
Aydin, A
von Treuenfels, N
Faulhaber, HD
Gohlke, HR
Knoblauch, H
Schuster, H
Luft, FC
Citation: A. Busjahn et al., Linkage but lack of association for blood pressure and the alpha-adducin locus in normotensive twins, J HYPERTENS, 17(10), 1999, pp. 1437-1441
Authors:
Knoblauch, H
Sommer, D
Zimmer, C
Tennstedt, C
Heling, K
Bollmann, R
Bommer, C
Tinschert, S
Korner, H
Citation: H. Knoblauch et al., Fetal trisomy 10 mosaicism: Ultrasound, cytogenetic and morphologic findings in early pregnancy, PRENAT DIAG, 19(4), 1999, pp. 379-382
Authors:
Busjahn, A
Knoblauch, H
Faulhaber, HD
Boeckel, T
Rosenthal, M
Uhlmann, R
Hoehe, M
Schuster, H
Luft, FC
Citation: A. Busjahn et al., QT interval is linked to 2 long-QT syndrome loci in normal subjects, CIRCULATION, 99(24), 1999, pp. 3161-3164
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
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