Zobrazeno 1 - 1
of 1
pro vyhledávání: '"I. V. Khavunka"'
Publikováno v:
Біологічні студії, Vol 8, Iss 1, Pp 45-52 (2014)
The clinical examination, genealogical and molecular genetic analysis of the probands and the risk group of three families with Peutz–Jeghers syndrome were carried out. The mutations of STK11 gene in exons 1, 2, 3 and 4, that lead to the formation
Externí odkaz:
https://doaj.org/article/c0d4ac366fc2439abc37cab86b4e0af4
