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The Korean Journal of Internal Medicine, ISSN 1226-3303, 03/2009, Volume 24, Issue 1, pp. 68 - 72
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 03/2007, Volume 282, Issue 13, p. 9941
Werner syndrome is a premature aging disease caused by mutations in the WS gene and a deficiency in the function of Werner protein (WRN). The lack of WRN... 
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 03/2007, Volume 282, Issue 13, pp. 9941 - 9951
Werner syndrome is a premature aging disease caused by mutations in the WS gene and a deficiency in the function of Werner protein (WRN). The lack of WRN... 
Journal Article
The Korean Journal of Internal Medicine, ISSN 1226-3303, 2009, Volume 24, Issue 1, p. 68
Hutchinson-Gilford progeria syndrome (HGPS) and Werner`s syndrome are representative types of progeroid syndrome. LMNA (Lamin A/C) gene mutation with atypical... 
LMNA | Progeroid syndrome | Werner`s syndrome | T506del
Journal Article
Book
Obstetrics and Gynecology Science, ISSN 2287-8572, 07/2017, Volume 60, Issue 4, pp. 374 - 377
Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly of the urogenital tract, which is characterized by the triad of uterus didelphys, obstructed... 
Urogenital anomalies | Renal agenesis | Herlyn-Werner-Wunderlich syndrome | Uterus didelphys | Case Report
Journal Article
2016, 1. Aufl., ISBN 3932338847, 317
Book
Book
by Khachatryan, V and Sirunyan, A M and Tumasyan, A and Adam, W and Bergauer, T and Dragicevic, M and Erö, J and Fabjan, C and Friedl, M and Frühwirth, R and Ghete, V M and Hartl, C and Hörmann, N and Hrubec, J and Jeitler, M and Kiesenhofer, W and Knünz, V and Krammer, M and Krätschmer, I and Liko, D and Mikulec, I and Rabady, D and Rahbaran, B and Rohringer, H and Schöfbeck, R and Strauss, J and Taurok, A and Treberer-Treberspurg, W and Waltenberger, W and Wulz, C.-E and Mossolov, V and Shumeiko, N and Suarez Gonzalez, J and Alderweireldt, S and Bansal, M and Bansal, S and Cornelis, T and De Wolf, E A and Janssen, X and Knutsson, A and Luyckx, S and Ochesanu, S and Rougny, R and Van De Klundert, M and Van Haevermaet, H and Van Mechelen, P and Van Remortel, N and Van Spilbeeck, A and Blekman, F and Blyweert, S and D’Hondt, J and Daci, N and Heracleous, N and Keaveney, J and Lowette, S and Maes, M and Olbrechts, A and Python, Q and Strom, D and Tavernier, S and Van Doninck, W and Van Mulders, P and Van Onsem, G P and Villella, I and Caillol, C and Clerbaux, B and De Lentdecker, G and Dobur, D and Favart, L and Gay, A P. R and Grebenyuk, A and Léonard, A and Mohammadi, A and Perniè, L and Reis, T and Seva, T and Thomas, L and Vander Velde, C and Vanlaer, P and Wang, J and Zenoni, F and Adler, V and Beernaert, K and Benucci, L and Cimmino, A and Costantini, S and Crucy, S and Dildick, S and Fagot, A and Garcia, G and Mccartin, J and Ocampo Rios, A A and Ryckbosch, D and Salva Diblen, S and Sigamani, M and Strobbe, N and Thyssen, F and Tytgat, M and Yazgan, E and Zaganidis, N and ... and CMS Collaboration and The CMS collaboration and Fermi National Accelerator Lab. (FNAL), Batavia, IL (United States)
Journal of High Energy Physics, ISSN 1126-6708, 10/2014, Volume 2014, Issue 10, pp. 1 - 54
Journal Article
Obstetrics & Gynecology Science, ISSN 2287-8572, 2017, Volume 60, Issue 4, p. 374
Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly of the urogenital tract, which is characterized by the triad of uterus didelphys, obstructed... 
Herlyn-Werner-Wunderlich syndrome; Renal agenesis; Urogenital anomalies; Uterus didelphys
Journal Article
by Chatrchyan, S and Khachatryan, V and Sirunyan, A M and Tumasyan, A and Adam, W and Bergauer, T and Dragicevic, M and Erö, J and Fabjan, C and Friedl, M and Frühwirth, R and Ghete, V M and Hartl, C and Hörmann, N and Hrubec, J and Jeitler, M and Kiesenhofer, W and Knünz, V and Krammer, M and Krätschmer, I and Liko, D and Mikulec, I and Rabady, D and Rahbaran, B and Rohringer, H and Schöfbeck, R and Strauss, J and Taurok, A and Treberer-Treberspurg, W and Waltenberger, W and Wulz, C.-E and Mossolov, V and Shumeiko, N and Suarez Gonzalez, J and Alderweireldt, S and Bansal, M and Bansal, S and Cornelis, T and De Wolf, E A and Janssen, X and Knutsson, A and Luyckx, S and Mucibello, L and Ochesanu, S and Roland, B and Rougny, R and Van Haevermaet, H and Van Mechelen, P and Van Remortel, N and Van Spilbeeck, A and Blekman, F and Blyweert, S and D’Hondt, J and Heracleous, N and Kalogeropoulos, A and Keaveney, J and Kim, T J and Lowette, S and Maes, M and Olbrechts, A and Strom, D and Tavernier, S and Van Doninck, W and Van Mulders, P and Van Onsem, G P and Villella, I and Caillol, C and Clerbaux, B and De Lentdecker, G and Favart, L and Gay, A P. R and Léonard, A and Marage, P E and Mohammadi, A and Perniè, L and Reis, T and Seva, T and Thomas, L and Vander Velde, C and Vanlaer, P and Wang, J and Adler, V and Beernaert, K and Benucci, L and Cimmino, A and Costantini, S and Dildick, S and Garcia, G and Klein, B and Lellouch, J and Mccartin, J and Ocampo Rios, A A and Ryckbosch, D and Salva Diblen, S and Sigamani, M and Strobbe, N and Thyssen, F and Tytgat, M and Walsh, S and Yazgan, E and ... and CMS Collaboration and The CMS collaboration and Fermi National Accelerator Lab. (FNAL), Batavia, IL (United States)
Journal of High Energy Physics, ISSN 1126-6708, 1/2014, Volume 2014, Issue 1, pp. 1 - 86
Journal Article
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