Showing 1 - 3 results of 3 for search 'Farzaneh Modarresi', query time: 0.02s Refine Results
  1. 1
    A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis

    A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis by Mohammad Reza Bordbar, Farzaneh Modarresi, Mohammad Ali Farazi Fard, Hassan Dastsooz, Nader Shakib Azad, Mohammad Ali Faghihi

    Published 2017
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  2. 2
    Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report

    Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report by Fatemeh Maghami, Seyed Mohammad Bagher Tabei, Hossein Moravej, Hassan Dastsooz, Farzaneh Modarresi, Mohammad Silawi, Mohammad Ali Faghihi

    Published 2018
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  3. 3
    Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene

    Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene by Parvaneh Karimzadeh, Samaneh Naderi, Farzaneh Modarresi, Hassan Dastsooz, Hamid Nemati, Tayebeh Farokhashtiani, Bibi Shahin Shamsian, Soroor Inaloo, Mohammad Ali Faghihi

    Published 2017
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