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Nature Communications|July 31, 2019
ER-residential Nogo-B accelerates NAFLD-associated HCC mediated by metabolic reprogramming of oxLDL lipophagyYuan Tian, Bin Yang, Weinan Qiu, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
22q13.3 deletion syndrome: clinical and molecular analysis using array CGHS U Dhar, D del Gaudio, J R German, et al.
Heart Rhythm|April 5, 2020
Guidance for cardiac electrophysiology during the COVID-19 pandemic from the Heart Rhythm Society COVID-19 Task Force; Electrophysiology Section of the American College of Cardiology; and the Electrocardiography and Arrhythmias Committee of the Council on Clinical Cardiology, American Heart AssociationDhanunjaya R Lakkireddy, Mina K Chung, Rakesh Gopinathannair, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|June 4, 2011
A synopsis of current haemophilia care in Hong KongW Y Au, Vincent Lee, Bonnie Kho, et al.
Genome Research|January 6, 2011
Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomesZhishuo Ou, Paweł Stankiewicz, Zhilian Xia, et al.
Gigascience|July 11, 2015
Erratum: SOAPdenovo2: an empirically improved memory-efficient short-read de novo assemblerRuibang Luo, Binghang Liu, Yinlong Xie, et al.
Journal of Medical Genetics|July 9, 2009
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairmentS C Sreenath Nagamani, F Zhang, O A Shchelochkov, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|February 25, 2021
Extracorporeal Membrane Oxygenation for Coronavirus Disease 2019: Crisis Standards of CareCara Agerstrand, Richard Dubois, Koji Takeda, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 16, 2019
Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayBettina E Mucha, Siddharth Banka, Norbert Fonya Ajeawung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2018
A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayBettina E Mucha, Siddharth Banka, Norbert Fonya Ajeawung, et al.
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