Showing results 1 to 4 of 4
Title | Author(s) | Issue Date | |
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CFTR: I1023R is a rare but recurrent disease-causing mutation found in Chinese patients with cystic fibrosis Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014 | 2014 | ||
Identification of a CFTR founder mutations, c.3068T>G:p.I1023R, which causes protein trafficking defects in Chinese patients with cystic fibrosis Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016 | 2016 | ||
Mode of delivery and childhood hospitalizations for asthma: evidence from the "Children of 1997" birth cohort Proceeding/Conference:HKCCM 2014 Annual Scientific Meeting & Fellowship Conferment Ceremony | 2014 | ||
Working memory in children with obstructive sleep apnea Proceeding/Conference:Neuroscience 2010 | 2010 |