|
发表于 2022-12-8 21:16:37
|
显示全部楼层
Women who are known to carry or are first degree untested relatives of individuals with less common disease causing mutations such as those associated with Li Fraumeni syndrome, Bannayan Riley Ruvalcaba syndrome, hereditary diffuse gastric cancer, Peutz Jeghers syndrome, Cowden syndrome, Neurofibromatosis type 1, or Fanconi anemia are also recommended for annual screening MRI beginning between ages 20 35, depending on the mutation <a href=https://clomid.one>buy provera and clomid online</a> |
|