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International Journal of Pediatric Otorhinolaryngology|October 20, 2015
Day-case adenotonsillectomy for sleep apnoea in children?Richard Wei Chern Gan, Tawakir Kamani, Sophie Wilkinson, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 11, 2020
Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosumChih-Ping Chen, Chin-Yuan Hsu, Schu-Rern Chern, et al.
Clinical Anatomy (New York, N.Y.)|January 19, 2018
Embryology of the craniocervical junction and posterior cranial fossa, part I: Development of the upper vertebrae and skullMohammadali M Shoja, Rebecca Ramdhan, Chad J Jensen, et al.
The Journal of Physical Chemistry. A|November 30, 2020
Stochastically Realized Observables for Excitonic Molecular AggregatesNadine C Bradbury, Chern Chuang, Arundhati P Deshmukh, et al.
Auris, Nasus, Larynx|January 20, 2021
Hydroacoustic analysis and extraluminal compression surgical insights of venous pulsatile tinnitusYue-Lin Hsieh, Xiaobing Xu, Yue-Da Hsieh, et al.
JMIR Mental Health|April 20, 2022
Behavioral Health Professionals' Perceptions on Patient-Controlled Granular Information Sharing (Part 1): Focus Group StudyJulia Ivanova, Tianyu Tang, Nassim Idouraine, et al.
Journal of Geophysical Research. Atmospheres : JGR|August 18, 2020
High-resolution NU-WRF simulations of a deep convective-precipitation system during MC3E: Further improvements and comparisons between Goddard microphysics schemes and observationsWei-Kuo Tao, Di Wu, Stephen Lang, et al.
Genetic Counseling (Geneva, Switzerland)|October 18, 2012
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type IIIC P Chen, S P Lin, Y N Suo, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|March 24, 2023
Mapping the Central Sulcus Extraoperatively Using Stereoelectroencephalography: A New Application of an Established MethodAmmar Kheder, Ruba Al-Ramadhani, Sonam Bhalla, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 10, 2021
Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly, ventricular septal defect, arthrogryposis of bilateral wrists and aplasia of the thumbsChih-Ping Chen, Shih-Shien Weng, Schu-Rern Chern, et al.
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