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of 4
pro vyhledávání: '"Bart Mol"'
Autor:
Laura C Gomez, Gabriela De Marchi, Diego M. Marzese, Bart Mol, Diego Bertani, Jorge Ibarra, Ivonne Johanna Vos, María Roqué, Jose Adi
Publikováno v:
Familial Cancer, 8(1), 67-73. SPRINGER
Colorectal cancer (CC) is the secondary cause of death in the Western countries of which approximately 15% are considered to be hereditary. The hereditary forms are Familial Adenomatous Polyposis (FAP) and Hereditary Non Polyposis Colorectal Cancer (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ee0707c696af231cc73b25b7428cade
https://doi.org/10.1007/s10689-008-9200-1
https://doi.org/10.1007/s10689-008-9200-1
Autor:
Yvonne J. Vos, Han G. Brunner, Gretel G. Oudesluijs, Annemarie H. van der Hout, Joke B. G. M. Verheij, Bart Mol, Patrick Rump, Andrea Venema, Anthonie J. van Essen
Publikováno v:
European Journal of Human Genetics, 16(6), 673-679. Nature Publishing Group
Hypohidrotic ectodermal dysplasia (HED) can be caused by mutations in the X-linked ectodysplasin A (ED1) gene or the autosomal ectodysplasin A-receptor (EDAR) and EDAR-associated death domain (EDARADD) genes. X-linked and autosomal forms are sometime
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cba14f2c9177ad90cf3ff76fa3c0ae43
https://doi.org/10.1038/sj.ejhg.5202012
https://doi.org/10.1038/sj.ejhg.5202012
Autor:
Huub J C van der Mijle, Bart Mol, Monique de Raad, Arend Karrenbeld, Yvonne J. Vos, Rolf H. Sijmons, Rein P. Stulp
Publikováno v:
World Journal of Gastroenterology, 12(5), 809-811. Baishideng Publishing Group Inc.
Hereditary non-polyposis colorectal carcinoma (HNPCC) is an autosomal dominant disorder associated with colorectal and endometrial cancer and a range of other tumor types. Germline mutations in the DNA mismatch repair (MMR) genes, particularly MLH1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdab96cfd79b2ccc18d8e0ef49114a93
https://pubmed.ncbi.nlm.nih.gov/16521201
https://pubmed.ncbi.nlm.nih.gov/16521201
Autor:
Bart Mol, Johanna C. Herkert, Rolf H. Sijmons, Yvonne J. Vos, Rein P. Stulp, Arend Karrenbeld
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 6, Iss 1, Pp 15-21 (2008)
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice
Lynch syndrome (HNPCC) is a dominantly inherited disorder characterized by germline defects in DNA mismatch repair (MMR) genes and the development of a variety of cancers, predominantly colorectal and endometrial. We present a 44-year-old woman who w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dad0513d508ff9364b94d64db778900b
https://doi.org/10.1186/1897-4287-6-1-15
https://doi.org/10.1186/1897-4287-6-1-15