Showing 1 - 4 results of 4 for search 'Saeid Morovvati', query time: 0.03s Refine Results
  1. 1
    CAD gene and early infantile epileptic encephalopathy-50; three Iranian deceased patients and a novel mutation: case report

    CAD gene and early infantile epileptic encephalopathy-50; three Iranian deceased patients and a novel mutation: case report by Sepideh Gholami Yarahmadi, Saeid Morovvati

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:
  2. 2
    Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness

    Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness by Sima Rayat, Mohammad Farhadi, Hessamaldin Emamdjomeh, Saeid Morovvati, Masoumeh Falah

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:
  3. 3
    Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation

    Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Mohammad Keramatipour, Saeid Morovvati

    Published 2021
    Connect to this object online.
    Book
    Save to List
    Saved in:
  4. 4
    Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report

    Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Aliagha Alishiri, Mohammad Keramatipour, Zeynab Javanfekr Shahri, Saeid Morovvati

    Published 2021
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: