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Information Journal Paper

Title

Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic Failure

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Pages

  86-89

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Abstract

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    APA: Copy

    . (2018). Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic Failure. Urology, 120(-), 86-89. SID. https://sid.ir/paper/754588/en

    Vancouver: Copy

    . Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic Failure. Urology[Internet]. 2018;120(-):86-89. Available from: https://sid.ir/paper/754588/en

    IEEE: Copy

    , “Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic Failure,” Urology, vol. 120, no. -, pp. 86–89, 2018, [Online]. Available: https://sid.ir/paper/754588/en

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