檢索結果 - Paracha, Sohail Aziz

  • Showing 1 - 2 results of 2
Refine Results
  1. 1
    Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder

    Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder 由 Mattioli, Francesca, Darvish, Hossein, Paracha, Sohail Aziz, Tafakhori, Abbas, Firouzabadi, Saghar Ghasemi, Chapi, Marjan, Baig, Hafiz Muhammad Azhar, Reymond, Alexandre, Antonarakis, Stylianos E., Ansar, Muhammad

    出版 2021
    獲取全文 獲取全文 獲取全文
    Text
    加到收藏夾
    Saved in:
  2. 2
    Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature

    Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature 由 Ansar, Muhammad, Paracha, Sohail Aziz, Serretti, Alessandro, Sarwar, Muhammad T, Khan, Jamshed, Ranza, Emmanuelle, Falconnet, Emilie, Iwaszkiewicz, Justyna, Shah, Sayyed Fahim, Qaisar, Azhar Ali, Santoni, Federico A, Zoete, Vincent, Megarbane, Andre, Ahmed, Jawad, Colombo, Roberto, Makrythanasis, Periklis, Antonarakis, Stylianos E

    出版 2019
    獲取全文 獲取全文 獲取全文
    Text
    加到收藏夾
    Saved in:

檢索工具: