Showing 1 - 8 results of 8 for search 'Nasrollah Saleh-Gohari', query time: 0.03s Refine Results
  1. 1
    Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient

    Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient by Nasrollah Saleh-gohari, Marzye Mohammadi-Anaie

    Published 2013-01-01
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  2. 2
    Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient

    Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient by Nasrollah Saleh-gohari, Marzye Mohammadi-Anaie

    Published 2013-02-01
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  3. 3
    Frequency of factor V Leiden (G1691A) and prothrombin (G20210A) polymorphisms in Population of Kerman Province, Iran

    Frequency of factor V Leiden (G1691A) and prothrombin (G20210A) polymorphisms in Population of Kerman Province, Iran by Nasrollah Saleh-gohari, Neda Salmani-Cheharfarsakhi

    Published 2017-09-01
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  4. 4
    Using nucleotide sequencing to determine HBV genotypes in Kerman

    Using nucleotide sequencing to determine HBV genotypes in Kerman by Najibe Monemi, Masoumeh Hajirezaei, Nasrollah Saleh-Gohari

    Published 2018-08-01
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  5. 5
    Haplotype Analysis in Carriers of β-Globin Gene Mutation Facil-itates Genetic Counseling in β-Thalassemia: A Cross-Sectional Study in Kerman Province, Iran

    Haplotype Analysis in Carriers of β-Globin Gene Mutation Facil-itates Genetic Counseling in β-Thalassemia: A Cross-Sectional Study in Kerman Province, Iran by Nasrollah SALEH-GOHARI, Kolsoum SAEIDI, Sima ZIAADINI-DASHTKHAKI

    Published 2020-04-01
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  6. 6
    The Association between Preeclampsia and Defined Polymorphisms in Prothrombin and Coagulation Factor V Genes

    The Association between Preeclampsia and Defined Polymorphisms in Prothrombin and Coagulation Factor V Genes by Zohreh Salari, Nasrollah Saleh-gohari, Nushin Zainali, Neda Salmani-Cheharfarsakhi

    Published 2016-09-01
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  7. 7
    Association between TNFα - 308 G/A and IFN-γ +874A/T polymorphisms with oral lichen planus

    Association between TNFα - 308 G/A and IFN-γ +874A/T polymorphisms with oral lichen planus by Nasrollah Saleh-gohari, molok torabi, Reihaneh Saleh Gohari, Elham Abbaszadeh, Malihe Saleh-gohari

    Published 2023-10-01
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  8. 8
    Homozygosity mapping and whole exome sequencing reveal a novel homozygous COL18A1 mutation causing Knobloch syndrome.

    Homozygosity mapping and whole exome sequencing reveal a novel homozygous COL18A1 mutation causing Knobloch syndrome. by Alireza Haghighi, Amit Tiwari, Niloofar Piri, Gudrun Nürnberg, Nasrollah Saleh-Gohari, Amirreza Haghighi, John Neidhardt, Peter Nürnberg, Wolfgang Berger

    Published 2014-01-01
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