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European Journal of Human Genetics : EJHG|August 9, 2012
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disordersSandesh C S Nagamani, Ayelet Erez, Bruria Ben-Zeev, et al.Journal of Foot and Ankle Research|August 12, 2025
Does Hallux Valgus Impair Medial Forefoot Loading? A Meta-Analysis of Plantar Pressure DistributionDuo Wai-Chi Wong, Esther Man-Wai Chow, Lucci Lugee Liyeung, et al.Data in Brief|June 7, 2021
Human tear proteome dataset in response to daily wear of water gradient contact lens using SWATH-MS approachJimmy Ka-Wai Cheung, Jingfang Bian, Ying-Hon Sze, et al.Clinical Cardiology|March 15, 2011
Type A aortic intramural hematoma: clinical features and outcomes in Chinese patientsHee Hwa Ho, Chi Wai Cheung, Man Hong Jim, et al.NPJ Science of Learning|May 6, 2026
Lab perceptual training and robot-assisted training in improving speech prosody of autistic childrenSi Chen, Bruce Xiao Wang, James Chung-Wai Cheung, et al.Trials|April 9, 2024
Effects of cognitive behavioural therapy and bright light therapy for insomnia in youths with eveningness: study protocol for a randomised controlled trialShirley Xin Li, Forrest Tin Wai Cheung, Ngan Yin Chan, et al.Journal of Medical Genetics|October 6, 2010
Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond--Blackfan anaemiaMargaret J Wat, Victoria B Enciso, Wojciech Wiszniewski, et al.Journal of Pediatric Surgery|April 16, 2013
Simple maneuvers to reduce the incidence of false-negative findings for contralateral patent processus vaginalis during laparoscopic hernia repair in children: a comparative study between 2 cohortsYuk Him Tam, Yuen Shan Wong, Kin Wai Chan, et al.Prenatal Diagnosis|September 17, 2008
Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGHWeimin Bi, Amy M Breman, Susan F Venable, et al.The Journal of Molecular Diagnostics : JMD|March 28, 2009
Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNASvetlana A Yatsenko, Chad A Shaw, Zhishuo Ou, et al.Pageof 60