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A novel KIF11 missense mutation causing Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR): A case report and literature review

6532-6547 2024-06-30

Samira Asadollahi, Fatemeh Sefid, Masoumeh Askari, Seyed Ahmad Mohammadi, Hamid Reza Jahantigh, Mahtab Ordooei

Prevalence of TECTA and GJB2 mutations in Asian children with nonsyndromic hearing loss: A meta-analysis

5717-5725 2023-06-30

Phuong Thu Vu Hoang, Quang An Lam, Minh Xuan Ngo, Anh Thu Ha Nguyen, Thanh Vu Nguyen, Chung Thuy Tran Phan

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