Sökresultat - Yi Ning

Current Aspects in the Molecular Genetics and Diagnostics of Spinal Muscular Atrophy av Shu-Chin Chien, Yi-Ning Su

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PHOX2B Mutation in a Taiwanese Newborn with Congenital Central Hypoventilation Syndrome av Tzu-Chiang Wang, Yi-Ning Su, Ming-Chi Lai

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Lethal fetal stroke in utero av Tzu-Hung Lin, Chien-Nan Lee, Yi-Ning Su

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Pelizaeus-Merzbacher Disease, Easily Misdiagnosed as Cerebral Palsy: A Report of a Three-generation Family av Yen-Chun Chen, Wen-Chen Liang, Yi-Ning Su, Yuh-Jyh Jong

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Muscle quality index is associated with trouble sleeping: a cross-sectional population based study av Yanwei You, Yuquan Chen, Qi Zhang, Ning Yan, Yi Ning, Qiang Cao

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Lymphomatoid papulosis with DUSP22-IRF4 rearrangement on 6p25-3: A case report av Yi-Ning Mao, Jie-Yang Jhuang, Bo-Jung Chen, Yu-Hung Wu

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Prenatal diagnosis of microvillus inclusion disease av Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Pei-Chen Wu, Wayseen Wang

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Septic Shock after Intracervical Laminaria Insertion av Shin-Yu Lin, Wen-Fang Cheng, Yi-Ning Su, Chi-An Chen, Chien-Nan Lee

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A large-cohort study of 2971 cases of epulis: focusing on risk factors associated with recurrence av Na Zhao, Yelidana Yesibulati, Pareyida Xiayizhati, Yi-Ning He, Rong-Hui Xia, Xiang-Zhen Yan

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Split hand/foot malformations with microdeletions at chromosomes 7 and 19 detected using array comparative genomic hybridization av Chin-Jui Wu, Yi-Ning Su, Tzu-Hung Lin, Li-Hui Tseng, Kuang-Han Chao

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Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus ass... av Ya-Lien Hsueh, Yi-Ning Su, Hsin-Yu Lin, Chien-Nan Lee, Jin-Chung Shih

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Targeted inhibition of methicillin-resistant Staphylococcus aureus biofilm formation by a graphene oxide-loaded aptamer/berberine bifunctional complex av Yi Ning, Xiaoqi Wang, Pingan Chen, Shiwu Liu, Jue Hu, Rong Xiao, Ling Li, Fangguo Lu

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Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: Prenatal diagnosis and literature review av Chih-Ping Chen, Yi-Ning Su, Tzu-Hung Lin, Tung-Yao Chang, Jun-Wei Su, Wayseen Wang

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Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism av Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

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Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome av Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

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Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II av Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

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Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene av Chih-Ping Chen, Yi-Ning Su, Yu-Ting Chen, Wen-Lin Chen, Lee James Hsu, Wayseen Wang

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Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II av Chih-Ping Chen, Yi-Ning Su, Fang-Yu Hung, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

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Prenatal diagnosis of proximal femoral focal deficiency: A case report and literature review av Tzu-Hung Lin, Chi-Hsien Chung, Jin-Chung Shih, Chia-Hui Lin, Chien-Nan Lee, Yi-Ning Su

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Intraperitoneal and intracardiac transfusion of recurrent fetal erythroblastosis due to anti-M alloimmunization with unfavorable outcome av Tzu-Hung Lin, Jin-Chung Shih, Chia-Hui Lin, Shin-Yu Lin, Yi-Ning Su, Chien-Nan Lee

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