Hasil Pencarian - Randa Alkhalaf

  • Menampilkan 1 - 1 hasil dari 1
Perbaiki Hasil
  1. 1
    Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report

    Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report oleh Fuad Al Mutairi, Randa Alkhalaf, Abdullah Alkhorayyef, Fayhan Alroqi, Alyafee Yusra, Muhammad Umair, Fetaini Nouf, Amjad Khan, Alharbi Meshael, Aleidi Hamad, Alaujan Monira, Abdulaziz Asiri, Kheloud M. Alhamoudi, Majid Alfadhel

    Diterbitkan 2020-05-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: