Medium and Large Artery Aneurysms in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy von Tan, Sarah Ming Li, Chin, Hui‐Lin, Makmur, Andrew, Tan, Benjamin Y.Q.

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Childhood vaccinations: Hidden impact of COVID-19 on children in Singapore von Zhong, Youjia, Clapham, Hannah Eleanor, Aishworiya, Ramkumar, Chua, Ying Xian, Mathews, Jancy, Ong, Mabel, Wang, Jingji, Murugasu, Belinda, Chiang, Wen Chin, Lee, Bee Wah, Chin, Hui-Lin

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A clinical approach to diagnosis and management of mitochondrial myopathies von Chin, Hui-Lin, Lai, Poh San, Tay, Stacey Kiat Hong

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An infant with hair like fur of a teddy bear von Lin, Jeremy, Wang, Furene, Chin, Hui-Lin, Han, Velda

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Pitfalls in clinical genetics von Chin, Hui-Lin, Goh, Denise Li Meng

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An infant with hair like fur of a teddy bear von Lin, Jeremy, Wang, Furene, Chin, Hui‐lin, Han, Velda

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Mesenteric cysts, lymphatic leak, and cerebral cavernous malformation in a proband with KRIT1‐related disease von Moller‐Hansen, Ashley, Huynh, Stephanie, Boerkoel, Cornelius F., Chin, Hui‐Lin

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E2F1 promotes cell migration in hepatocellular carcinoma via FNDC3B von Hua, Kate, Wu, Chen‐Tang, Lin, Chin‐Hui, Chen, Chian‐Feng

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Long‐read genome sequencing resolves a complex 13q structural variant associated with syndromic anophthalmia von Boerkoel, Pierre K., Dixon, Katherine, Fitzsimons, Carrie, Shen, Yaoqing, Huynh, Stephanie, Schlade‐Bartusiak, Kamilla, Culibrk, Luka, Chan, Simon, Boerkoel, Cornelius F., Jones, Steven J. M., Chin, Hui‐Lin

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Non-immune hydrops fetalis caused by Diamond-Blackfan anaemia and a mutation of the RPL15 gene von Dashraath, Pradip, Lim, Karen M X, Chin, Hui-Lin, Sidek, Azleen, Lian, Derrick W Q, Gosavi, Arundhati, Koh, Pei Lin, Biswas, Arijit, Goh, Denise L M

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An approach to rapid characterization of DMD copy number variants for prenatal risk assessment von Chin, Hui‐Lin, O'Neill, Kieran, Louie, Kristal, Brown, Lindsay, Schlade‐Bartusiak, Kamilla, Eydoux, Patrice, Rupps, Rosemarie, Farahani, Ali, Boerkoel, Cornelius F., Jones, Steven J. M.

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An infant with congenital respiratory insufficiency and diaphragmatic paralysis: A novel BICD2 phenotype? von Chin, Hui‐Lin, Huynh, Stephanie, Ashkani, Jahanshah, Castaldo, Michael, Dixon, Katherine, Selby, Kathryn, Shen, Yaoqing, Wright, Marie, Boerkoel, Cornelius F., Hendson, Glenda, Jones, Steven J. M.

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Using gene panels in the diagnosis of neuromuscular disorders: A mini-review von Ng, Kay W. P., Chin, Hui-Lin, Chin, Amanda X. Y., Goh, Denise Li-Meng

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Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience von Chin, Hui-Lin, Lam, Joyce Ching Mei, Christopher, Dheepa, Michelle, Poon Limei, Junrong, Benedict Yan

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Subclinical Cardiomyopathy in Miyoshi Myopathy Detected by Late Gadolinium Enhancement Cardiac Magnetic Resonance Imaging: A Case for Routine Cardiac Screening? von Tan, Sarah Ming Li, Ong, Ching Ching, Tan, Kong Bing, Chin, Hui-Lin, Paliwal, Prakash R, Ng, Kay Wei Ping, Lin, Weiqin

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A combination of two novel VARS2 variants causes a mitochondrial disorder associated with failure to thrive and pulmonary hypertension von Chin, Hui-Lin, Goh, Denise Li-Meng, Wang, Furene Sijia, Tay, Stacey Kiat Hong, Heng, Chew Kiat, Donnini, Claudia, Baruffini, Enrico, Pines, Ophry

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Expression Profiling of Exosomal miRNAs Derived from the Aqueous Humor of Myopia Patients von Chen, Chian-Feng, Hua, Kate, Woung, Lin-Chung, Lin, Chin-Hui, Chen, Chueh-Tan, Hsu, Chung-Hua, Liou, Shiow-Wen, Tsai, Ching-Yao

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Genetics in Ischemic Stroke: Current Perspectives and Future Directions von Zhang, Ka, Loong, Shaun S E, Yuen, Linus Z H, Venketasubramanian, Narayanaswamy, Chin, Hui-Lin, Lai, Poh San, Tan, Benjamin Y Q

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Changes in interferon-γ release assay readout after COVID-19 vaccination: A prospective cohort study von Chen, Nan-Yu, Liu, Zhuo-Hao, Kao, Shu-Wei, Lin, Huang-Shen, Lee, Ing-Kit, Zheng, Jun-Yuan, Wang, Ssu-Wei, Hsiao, Yu-Hsiang, Lin, Hui-Chin, Wu, Ting-Shu

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Clinical application of targeted long read sequencing in prenatal beta‐thalassemia testing and genetic counseling von Chin, Hui‐Lin, Benton, Miles C., Yang, Lin, Poon, Kok Siong, Tan, Karen M. L., Jamuar, Saumya S., Foo, Roger, Law, Hai Yang, Goh, Denise Li‐Meng, Chong, Samuel S., Sessions, Paola Florez

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