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Springer Nature3
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✓Human Genetics3
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20121
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Hui-Ching Lin results 3 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Hui-Ching Lin ×Clear All Filters
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Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening eventsNARA Subscribed
Human Genetics · 2012 · Vol. 131 · Issue 8 · Springer
Shuenn-Nan Chiu; Mei-Hwan Wu; Ming-Jai Su; Jou-Kou Wang; Ming-Tai Lin; Chien-Chih Chang; Hui-Wen Hsu; Ching-Tsuen Shen; Olivier Thériault; Mohamed Chahine
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Erratum to: Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing lossNARA Subscribed
Human Genetics · 2010 · Vol. 127 · Issue 5 · Springer
Hui-Mei Hong; Jiann-Jou Yang; Jia-Ching Shieh; Mei-Ling Lin; Shuan-Yow Li
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Microsatellite polymorphism in promoter of heme oxygenase-1 gene is associated with susceptibility to coronary artery disease in type 2 diabetic patientsNARA Subscribed
Human Genetics · 2002 · Vol. 111 · Issue 1 · Springer
Ying-Hwa Chen; Shing-Jong Lin; Ming-Wei Lin; Hui-Ling Tsai; San-San Kuo; Jaw-Wen Chen; Min-Ji Charng; Tao-Cheng Wu; Lung-Ching Chen; Philip Ding; Wen-Harn Pan; Yuh-Shan Jou; Lee-Young Chau
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