Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Hkp vanAmstel"'
Autor:
Chang X. Zhang, Mark I. McCarthy, Wjm VandeVen, Patrick Gaudray, Rajesh V. Thakker, Andrew P. Read, Simon A. Forbes, Cjm Lips, Sophie Giraud, Soili Kytölä, Alain Calender, J. Leisti, Jwm Hoppener, Koen Kas, Catharina Larsson, Hkp vanAmstel, Bin Tean Teh, Aaj Pannett, Pasi I. Salmela, Günther Weber, Jhd Bassett
Publikováno v:
Human Genetics. 100:657-665
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by tumours of the parathyroids, pancreas and anterior pituitary. The MEN1 gene has been localised to a 2-Mb region of chromosome 11q13 by meiotic mapping studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c3fa22108f65a327aee62f8f335155a
https://doi.org/10.1007/s004390050569
https://doi.org/10.1007/s004390050569
Publikováno v:
HUMAN GENETICS, 97(1), 11-14. SPRINGER
Hereditary C-cell carcinoma is encountered in multiple endocrine neoplasia type 2A (MEN 2A), MEN 2B, and familial medullary thyroid carcinoma (FMTC). Mutations of the RET proto-oncogene are associated with all three diseases. To obtain an insight int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da08b9498d73b04f89f0af18d3a9512d
https://doi.org/10.1007/bf00218825
https://doi.org/10.1007/bf00218825