Search Results - Shankar, Aissvarya

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  1. 1
    Biallelic variants in GLB1 causes GM1-gangliosidosis disease in a family with two siblings

    Biallelic variants in GLB1 causes GM1-gangliosidosis disease in a family with two siblings by Karuppiah, Thilakavathy, Ling, King Hwa, Lim, Chong Teik, Shankar, Aissvarya, Thong, Meow Keong, Abdul Aziz, Noraishah Mydin

    Published 2024
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  2. 2
    Integrative bioinformatics analysis and whole exome sequencing reveal differentially expressed genes and single nucleotide polymorphisms in Dupuytren’s contracture

    Integrative bioinformatics analysis and whole exome sequencing reveal differentially expressed genes and single nucleotide polymorphisms in Dupuytren’s contracture by Karuppiah, Thilakavathy, Arumugam, Manohar, Hwa, Ling King, Shankar, Aissvarya

    Published 2024
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  3. 3
    Variant identification using whole exome sequencing in a family suspected with Iron-refractory Iron Deficiency Anaemia

    Variant identification using whole exome sequencing in a family suspected with Iron-refractory Iron Deficiency Anaemia by Karuppiah, Thilakavathy, Mohamed Ibrahim, Noor Haliza, Musa, Nurul Huda, Shankar, Aissvarya, Ahmad Asnawi, Asral Wirda, Yap, Mandy Yee Yee, Sathar, Jameela, Selvaratnam, Veena, Noor Alif Wira, Nurul Ain Suraya

    Published 2024
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