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Hui-Lin Chin

Showing results (11-20 of 36) with videos related to

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Frontiers in Oncology|October 20, 2023
Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling-a Singaporean experienceHui-Lin Chin, Joyce Ching Mei Lam, Dheepa Christopher, et al.
Frontiers in Neurology|October 31, 2022
Using gene panels in the diagnosis of neuromuscular disorders: A mini-reviewKay W P Ng, Hui-Lin Chin, Amanda X Y Chin, et al.
Frontiers in Pediatrics|August 27, 2025
Case Report: Incidental diagnosis of cystic fibrosis via whole genome sequencing alters HSCT planning in a child with cerebral X-linked adrenoleukodystrophyJann Adriel Chua Sy, Poh Lin Tan, Jeremy Bingyuan Lin, et al.
The Lancet. Rheumatology|January 24, 2024
Covert Ehlers-Danlos syndrome in pregnancyPradip Dashraath, Soe-Na Choo, Harvard Lin, et al.
Thrombosis Journal|January 12, 2017
The genetic variation rs6903956 in the novel androgen-dependent tissue factor pathway inhibitor regulating protein (<i>ADTRP</i>) gene is not associated with levels of plasma coagulation factors in the Singaporean ChineseXuling Chang, Hui-Lin Chin, Swee-Chye Quek, et al.
Neurology. Genetics|May 9, 2025
Atypical Presentation of an <i>LMNB1</i> Duplication Involving the Silencer Region: Beyond Classical Autosomal-Dominant LeukodystrophyJia Dong James Wang, Tamara N Kimball, Savvina Prapiadou, et al.
Journal of Cardiovascular Development and Disease|December 22, 2023
Genetics in Ischemic Stroke: Current Perspectives and Future DirectionsKa Zhang, Shaun S E Loong, Linus Z H Yuen, et al.
Journal of Molecular Medicine (Berlin, Germany)|September 19, 2019
A combination of two novel VARS2 variants causes a mitochondrial disorder associated with failure to thrive and pulmonary hypertensionHui-Lin Chin, Denise Li-Meng Goh, Furene Sijia Wang, et al.
American Journal of Medical Genetics. Part A|May 21, 2021
An approach to rapid characterization of DMD copy number variants for prenatal risk assessmentHui-Lin Chin, Kieran O'Neill, Kristal Louie, et al.
European Journal of Medical Genetics|January 22, 2022
Can leaky splicing and evasion of premature termination codon surveillance contribute to the phenotypic variability in Alkuraya-Kucinskas syndrome?Hui-Lin Chin, Susan Lin, Joshua Dalmann, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Frontiers in Oncology|October 20, 2023
Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling-a Singaporean experienceHui-Lin Chin, Joyce Ching Mei Lam, Dheepa Christopher, et al.
Frontiers in Neurology|October 31, 2022
Using gene panels in the diagnosis of neuromuscular disorders: A mini-reviewKay W P Ng, Hui-Lin Chin, Amanda X Y Chin, et al.
Frontiers in Pediatrics|August 27, 2025
Case Report: Incidental diagnosis of cystic fibrosis via whole genome sequencing alters HSCT planning in a child with cerebral X-linked adrenoleukodystrophyJann Adriel Chua Sy, Poh Lin Tan, Jeremy Bingyuan Lin, et al.
The Lancet. Rheumatology|January 24, 2024
Covert Ehlers-Danlos syndrome in pregnancyPradip Dashraath, Soe-Na Choo, Harvard Lin, et al.
Thrombosis Journal|January 12, 2017
The genetic variation rs6903956 in the novel androgen-dependent tissue factor pathway inhibitor regulating protein (<i>ADTRP</i>) gene is not associated with levels of plasma coagulation factors in the Singaporean ChineseXuling Chang, Hui-Lin Chin, Swee-Chye Quek, et al.
Neurology. Genetics|May 9, 2025
Atypical Presentation of an <i>LMNB1</i> Duplication Involving the Silencer Region: Beyond Classical Autosomal-Dominant LeukodystrophyJia Dong James Wang, Tamara N Kimball, Savvina Prapiadou, et al.
Journal of Cardiovascular Development and Disease|December 22, 2023
Genetics in Ischemic Stroke: Current Perspectives and Future DirectionsKa Zhang, Shaun S E Loong, Linus Z H Yuen, et al.
Journal of Molecular Medicine (Berlin, Germany)|September 19, 2019
A combination of two novel VARS2 variants causes a mitochondrial disorder associated with failure to thrive and pulmonary hypertensionHui-Lin Chin, Denise Li-Meng Goh, Furene Sijia Wang, et al.
American Journal of Medical Genetics. Part A|May 21, 2021
An approach to rapid characterization of DMD copy number variants for prenatal risk assessmentHui-Lin Chin, Kieran O'Neill, Kristal Louie, et al.
European Journal of Medical Genetics|January 22, 2022
Can leaky splicing and evasion of premature termination codon surveillance contribute to the phenotypic variability in Alkuraya-Kucinskas syndrome?Hui-Lin Chin, Susan Lin, Joshua Dalmann, et al.
Pageof 4