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Ophthalmic Genetics|July 14, 2022
Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosomeSandra Hoyek, Marlene Wang, Audina M Berrocal, et al.
Birth Defects Research|June 22, 2017
Assisted Reproductive Technology and Birth Defects: Effects of Subfertility and Multiple BirthsRebecca F Liberman, Kelly D Getz, Dominique Heinke, et al.
The Journal of Hospital Infection|July 6, 2014
From SARS in 2003 to H1N1 in 2009: lessons learned from Taiwan in preparation for the next pandemicM-Y Yen, A W-H Chiu, J Schwartz, et al.
Journal of Pediatric Orthopedics|October 12, 2020
Universal Screening for COVID-19 in Children Undergoing Orthopaedic Surgery: A Multicenter ReportTodd J Blumberg, Adam C Adler, Elaina E Lin, et al.
Toxins|November 10, 2011
Bacterial heat-stable enterotoxins: translation of pathogenic peptides into novel targeted diagnostics and therapeuticsJieru E Lin, Michael Valentino, Glen Marszalowicz, et al.
American Journal of Medical Genetics|May 14, 1999
Cardiovascular malformations: changes in prevalence and birth status, 1972-1990A E Lin, A H Herring, K S Amstutz, et al.
Organic Letters|October 20, 2017
Three-Component Catalytic Carboxygenation of Activated Alkenes Enabled by Bimetallic Rh(III)/Cu(II) CatalysisShang-Shi Zhang, Jie Xia, Jia-Qiang Wu, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 1, 2017
Imaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spacesP F Sinnige, C M A van Ravenswaaij-Arts, P Caruso, et al.
Angewandte Chemie (International Ed. in English)|October 26, 2018
gem-Difluorination of Alkenyl N-methyliminodiacetyl Boronates: Synthesis of α- and β-Difluorinated AlkylboronsWen-Xin Lv, Qingjiang Li, Ji-Lin Li, et al.
American Journal of Medical Genetics|April 15, 2000
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndromeA E Lin, E V Semina, S Daack-Hirsch, et al.
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