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pro vyhledávání: '"Daniel E.J. Waschk"'
To date, a disease-causing mutation can be found in approximately 15-30% of families with hereditary breast and ovarian cancer and still more than half of the cases remain unsolved. Usually it is intended to perform genetic analyses in the family mem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64c0093135ca834f5b7020077eb6fc2f
https://doi.org/10.1101/527168
https://doi.org/10.1101/527168
Autor:
Melih Bayat, Daniel E.J. Waschk, Carla Herden, Ye Wang, Eva Liebau, Erik C. Andersen, Robyn E. Tanny, Jens Daniel
Publikováno v:
Gene. 732:144367
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ab2d268eb4208ca66bb278f24ffa839
https://doi.org/10.1016/j.gene.2020.144367
https://doi.org/10.1016/j.gene.2020.144367
Autor:
Karina Kapczuk, Peter Hillemanns, Ann-Christin Tewes, Susanne Ledig, J. Hucke, Daniel E.J. Waschk, Thomas Römer, Cordula Schippert, Peter Wieacker
Publikováno v:
Clinical Genetics. 89:590-596
Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS) is a well-known malformation pattern of the Mullerian ducts (MDs) characterized by congenital absence of the uterus and vagina. To date, most cases remain unexplained at molecular level. As female Wnt9b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61d09d57999c7d9486892761ec7747b8
https://doi.org/10.1111/cge.12701
https://doi.org/10.1111/cge.12701