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Showing 1 - 4 results of 4 for search 'Hane Lee', query time: 0.02s Refine Results
  1. 1
    Correction: whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature

    Correction: whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical fea... by Atefeh Mir, Yongjun Song, Hane Lee, Hossein Khanahmad, Erfan Khorram, Jafar Nasiri, Mohammad Amin Tabatabaiefar

    Published 2025-02-01
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  2. 2
    Developing a disease-specific accessible transcriptional signature as a biomarker for ataxia with oculomotor apraxia type 2

    Developing a disease-specific accessible transcriptional signature as a biomarker for ataxia with oculomotor apraxia type 2 by Kathie J. Ngo, Darice Y. Wong, Alden Y. Huang, Hane Lee, Stanley F. Nelson, Brent L. Fogel

    Published 2025-05-01
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  3. 3
    A first large study of whole-exome sequencing (WES) in 489 patients with suspected rare genetic disorders at a tertiary centre in Malaysia

    A first large study of whole-exome sequencing (WES) in 489 patients with suspected rare genetic disorders at a tertiary centre in Malaysia by Lip Hen Moey, Go Hun Seo, Boon Eu Cheah, Wee Teik Keng, Hane Lee, Gaik Siew Ch’ng

    Published 2025-01-01
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  4. 4
    RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis

    RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis by Samantha Wong, Yu Xuan Tan, Abigail Yi Ting Loh, Kiat Yi Tan, Hane Lee, Zainab Aziz, Stanley F Nelson, Engin Özkan, Hülya Kayserili, Nathalie Escande‐Beillard, Bruno Reversade

    Published 2023-04-01
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