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Author Details
Full Name
Hui-Lin Chin
Affiliation
Yong Loo Lin School of Medicine, National University of Singapore
ORCID
Career Start Year
2015
Papers
20
H Index
4
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37740604
Clinical application of targeted long read sequencing in prenatal beta-thalassemia testing and genetic counseling.
Mol Genet Genomic Med
2024
36714130
The practice of genomic medicine: A delineation of the process and its governing principles.
Front Med (Lausanne)
2023
37422302
Non-immune hydrops fetalis caused by Diamond-Blackfan anaemia and a mutation of the RPL15 gene.
Lancet
2023
36722517
Pitfalls in clinical genetics.
Singapore Med J
2023
34558799
Mesenteric cysts, lymphatic leak, and cerebral cavernous malformation in a proband with KRIT1-related disease.
Am J Med Genet A
2022
35442193
The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice.
Genet Med
2022
36468525
An infant with hair like fur of a teddy bear.
J Paediatr Child Health
2022
36313509
Using gene panels in the diagnosis of neuromuscular disorders: A mini-review.
Front Neurol
2022
35122461
Long-read genome sequencing resolves a complex 13q structural variant associated with syndromic anophthalmia.
Am J Med Genet A
2022
35063693
Can leaky splicing and evasion of premature termination codon surveillance contribute to the phenotypic variability in Alkuraya-Kucinskas syndrome?
Eur J Med Genet
2022
34825470
An infant with congenital respiratory insufficiency and diaphragmatic paralysis: A novel BICD2 phenotype?
Am J Med Genet A
2022
32819910
Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management.
Arch Dis Child
2021
33518658
Subclinical Cardiomyopathy in Miyoshi Myopathy Detected by Late Gadolinium Enhancement Cardiac Magnetic Resonance Imaging.
Int Heart J
2021
34018669
An approach to rapid characterization of DMD copy number variants for prenatal risk assessment.
Am J Med Genet A
2021
33414050
Childhood vaccinations: Hidden impact of COVID-19 on children in Singapore.
Vaccine
2021
32045119
An infant with hair like fur of a teddy bear.
J Paediatr Child Health
2020
29668551
Fetal-onset Congenital Dyserythropoietic Anemia Type 1 due to a Novel Mutation With Severe Iron Overload and Severe Cholestatic Liver Disease.
J Pediatr Hematol Oncol
2019
31529142
A combination of two novel VARS2 variants causes a mitochondrial disorder associated with failure to thrive and pulmonary hypertension.
J Mol Med (Berl)
2019
28074087
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 Chinese.
Thromb J
2017
26937410
Two consecutive partial liver transplants in a patient with Classic Maple Syrup Urine Disease.
Mol Genet Metab Rep
2015
1 - 20 of 20
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