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NARA Subscribed2
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Springer Nature2
Journal
✓Human Genetics2
Publication Year
20191
20101
Li-Ching Chang results 2 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Li-Ching Chang ×Clear All Filters
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Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing dataNARA Subscribed
Human Genetics · 2019 · Vol. 138 · Issue 2 · Springer
Karen Y. He; Xiaoyin Li; Tanika N. Kelly; Jingjing Liang; Brian E. Cade; Themistocles L. Assimes; Lewis C. Becker; Amber L. Beitelshees; Adam P. Bress; Yen-Pei Christy Chang; Yii-Der Ida Chen; Paul S. de Vries; Ervin R. Fox; Nora Franceschini; Anna Furniss; Yan Gao; Xiuqing Guo; Jeffrey Haessler; Shih-Jen Hwang; Marguerite Ryan Irvin; Rita R. Kalyani; Ching-Ti Liu; Chunyu Liu; Lisa Warsinger Martin; May E. Montasser; Paul M. Muntner; Stanford Mwasongwe; Walter Palmas; Alex P. Reiner; Daichi Shimbo; Jennifer A. Smith; Beverly M. Snively; Lisa R. Yanek; Eric Boerwinkle; Adolfo Correa; L. Adrienne Cupples; Jiang He; Sharon L. R. Kardia; Charles Kooperberg; Rasika A. Mathias; Braxton D. Mitchell; Bruce M. Psaty; Ramachandran S. Vasan; D. C. Rao; Stephen S. Rich; Jerome I. Rotter; James G. Wilson; Aravinda Chakravarti; Alanna C. Morrison; Daniel Levy; Donna K. Arnett; Susan Redline; Xiaofeng Zhu
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A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing lossNARA Subscribed
Human Genetics · 2010 · Vol. 127 · Issue 2 · Springer
Hui-Mei Hong; Jiann-Jou Yang; Ching-Chyuan Su; Juan-Yu Chang; Tung-Cheng Li; Shuan-Yow Li
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