Hasil Pencarian - Prakash Chermakani

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  1. 1
    Traboulsi syndrome: A rare eye disease and its genetic association

    Traboulsi syndrome: A rare eye disease and its genetic association oleh Prakash Chermakani, Periasamy Sundaresan

    Diterbitkan 2023-01-01
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  2. 2
    Exploring mito-nuclear genetic factors in Leber's hereditary optic neuropathy

    Exploring mito-nuclear genetic factors in Leber's hereditary optic neuropathy oleh Prakash Chermakani, Poigaialwar Gowri, Shanmugam Mahesh Kumar, Periasamy Sundaresan

    Diterbitkan 2023-10-01
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  3. 3
    Genotypic and phenotypic diversity in X-linked retinoschisis: Findings from a South Indian patient cohort

    Genotypic and phenotypic diversity in X-linked retinoschisis: Findings from a South Indian patient cohort oleh Susmita Chowdhury, Prakash Chermakani, Girish Baliga, Rupa Anjanamurthy, Periasamy Sundaresan

    Diterbitkan 2024-02-01
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  4. 4
    Genetic characterization of Stargardt clinical phenotype in South Indian patients using sanger and targeted sequencing

    Genetic characterization of Stargardt clinical phenotype in South Indian patients using sanger and targeted sequencing oleh Rajendran Kadarkarai Raj, Pankaja Dhoble, Rupa Anjanamurthy, Prakash Chermakani, Manojkumar Kumaran, Bharanidharan Devarajan, Periasamy Sundaresan

    Diterbitkan 2020-01-01
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  5. 5
    Whole-exome sequencing identifies multiple pathogenic variants in a large South Indian family with primary open-angle glaucoma

    Whole-exome sequencing identifies multiple pathogenic variants in a large South Indian family with primary open-angle glaucoma oleh Mohd Hussain Shah, Manojkumar Kumaran, Prakash Chermakani, Mohideen Abdul Kader, R Ramakrishnan, Subbiah R Krishnadas, Bharanidharan Devarajan, Periasamy Sundaresan

    Diterbitkan 2021-01-01
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