Categoría: ORIGINAL ARTICLE
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Clinical application of prospective whole‐exome sequencing in the diagnosis of genetic disease: Experience of a regional disease center in South Korea
Annals of Human Genetics, Volume 88, Issue 2, Page 101-112, March 2024.
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The effect of TRIM5 variants on the susceptibility to HIV‐1 infection and disease progression in the Polish population
Annals of Human Genetics, Volume 88, Issue 2, Page 154-170, March 2024.
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Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting
Annals of Human Genetics, Volume 88, Issue 2, Page 113-125, March 2024.
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Association of blood lipid profiles and asthma: A bidirectional two‐sample Mendelian randomization study
Annals of Human Genetics, EarlyView.
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ABCA1 variant rs9282541 is associated with metabolic syndrome in Maya children
Annals of Human Genetics, EarlyView.
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Investigation of the association between the Toll‐like receptor 1 rs4833095 variation and gastric adenocarcinoma recurrence
Annals of Human Genetics, EarlyView.
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Exploring the clinical significance of miR‐148 expression variations in distinct subtypes of irritable bowel syndrome
Annals of Human Genetics, EarlyView.
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Expression analysis of NF1‐mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR
Annals of Human Genetics, EarlyView.