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Browsing by Author Saisuda Noojarern

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Showing results 1 to 3 of 3
Issue DateTitleAuthor(s)
1-Dec-2020Duox2 variants are a frequent cause of congenital primary hypothyroidism in thai patientsKinnaree Sorapipatcharoen; Thipwimol Tim-Aroon; Pat Mahachoklertwattana; Wasun Chantratita; Nareenart Iemwimangsa; Insee Sensorn; Bhakbhoom Panthan; Poramate Jiaranai; Saisuda Noojarern; Patcharin Khlairit; Sarunyu Pongratanakul; Chittiwat Suprasongsin; Manassawee Korwutthikulrangsri; Chutintorn Sriphrapradang; Preamrudee Poomthavorn; Faculty of Medicine, Ramathibodi Hospital, Mahidol University
1-Jan-2019Identification of Gene Mutations in Primary Pediatric Cardiomyopathy by Whole Exome SequencingKitiwan Rojnueangnit; Boonchu Sirichongkolthong; Ratthapon Wongwandee; Thanitchet Khetkham; Saisuda Noojarern; Arthaporn Khongkraparn; Duangrurdee Wattanasirichaigoon; Thammasat University Hospital; Faculty of Medicine, Ramathibodi Hospital, Mahidol University; Faculty of Medicine, Thammasat University
1-Dec-2020MITF variants cause nonsyndromic sensorineural hearing loss with autosomal recessive inheritanceSupranee Thongpradit; Natini Jinawath; Asif Javed; Saisuda Noojarern; Arthaporn Khongkraparn; Thipwimol Tim-Aroon; Krisna Lertsukprasert; Bhoom Suktitipat; Laran T. Jensen; Duangrurdee Wattanasirichaigoon; A-Star, Genome Institute of Singapore; Faculty of Medicine, Ramathibodi Hospital, Mahidol University; Mahidol University; Faculty of Medicine, Siriraj Hospital, Mahidol University; The University of Hong Kong