Search Results - Noavar, Sadaf

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  1. 1
    A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss

    A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss by Fahimi, Hossein, Behroozi, Samira, Noavar, Sadaf, Parvini, Farshid

    Published in BMC medical genomics
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  2. 2
    A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature

    A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature by Noavar, Sadaf, Behroozi, Samira, Tatarcheh, Taraneh, Parvini, Farshid, Foroutan, Majid, Fahimi, Hossein

    Published in BMC medical genetics
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