Hasil Pencarian - Min-Fei Pei

  • Menampilkan 1 - 1 hasil dari 1
Perbaiki Hasil
  1. 1
    An intron mutation in the ACVRL1 may be associated with a transcriptional regulation defect in a Chinese family with hereditary hemorrhagic telangiectasia.

    An intron mutation in the ACVRL1 may be associated with a transcriptional regulation defect in a Chinese family with hereditary hemorrhagic telangiectasia. oleh Qian Yu, Xiao-Hui Shen, Ying Li, Rui-Juan Li, Ji Li, Yun-Ya Luo, Su-Fang Liu, Ming-Yang Deng, Min-Fei Pei, Guang-Sen Zhang

    Diterbitkan 2013-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: