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Journal of Neonatal-Perinatal Medicine
|
April 11, 2022
Epidemiological evolution of early-onset neonatal sepsis over 12 years: A single center, population-based study in central Taiwan
I-Chun Lu, Yu-Chia Chang, Yin-Ting Chen, et al.
Orphanet Journal of Rare Diseases
|
December 3, 2015
Genotype and phenotype analysis of Taiwanese patients with osteogenesis imperfecta
Hsiang-Yu Lin, Chih-Kuang Chuang, Yi-Ning Su, et al.
Diagnostics (Basel, Switzerland)
|
October 24, 2020
Effect of Mutated <i>ids</i> Overexpression on IDS Enzyme Activity and Developmental Phenotypes in Zebrafish Embryos: A Valuable Index for Assessing Critical Point-Mutations Associated with Mucopolysaccharidosis Type II Occurrence in Humans
Cheng-Yung Lin, Hsiang-Yu Lin, Chih-Kuang Chuang, et al.
Journal of Personalized Medicine
|
July 27, 2022
Quantification of Idua Enzymatic Activity Combined with Observation of Phenotypic Change in Zebrafish Embryos Provide a Preliminary Assessment of Mutated <i>idua</i> Correlated with Mucopolysaccharidosis Type I
Cheng-Yung Lin, Hsiang-Yu Lin, Chih-Kuang Chuang, et al.
Journal of Personalized Medicine
|
July 27, 2022
Functional Independence of Taiwanese Children with Osteogenesis Imperfecta
Yu-Min Syu, Chung-Lin Lee, Chih-Kuang Chuang, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2
Hsiang-Yu Lin, Tina Jui-Ting Wu, Ju-Hui Hsu, et al.
Archives of Dermatological Research
|
April 7, 2007
Netherton syndrome: mutation analysis of two Taiwanese families
Shuan-Pei Lin, Shu-Yi Huang, Mei-Eng Tu, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
November 19, 2021
Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndrome
Chih-Ping Chen, Schu-Rern Chern, Chien-Hsing Lin, et al.
Journal of Clinical Ultrasound : JCU
|
March 22, 2007
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome
Chih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
April 29, 2008
Cri-du-chat syndrome
Chia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Page
of 19
Search research articles
Search
Showing results (61-70 of 183) with videos related to
Sort By:
Page
of 19
Journal of Neonatal-Perinatal Medicine
|
April 11, 2022
Epidemiological evolution of early-onset neonatal sepsis over 12 years: A single center, population-based study in central Taiwan
I-Chun Lu, Yu-Chia Chang, Yin-Ting Chen, et al.
Orphanet Journal of Rare Diseases
|
December 3, 2015
Genotype and phenotype analysis of Taiwanese patients with osteogenesis imperfecta
Hsiang-Yu Lin, Chih-Kuang Chuang, Yi-Ning Su, et al.
Diagnostics (Basel, Switzerland)
|
October 24, 2020
Effect of Mutated <i>ids</i> Overexpression on IDS Enzyme Activity and Developmental Phenotypes in Zebrafish Embryos: A Valuable Index for Assessing Critical Point-Mutations Associated with Mucopolysaccharidosis Type II Occurrence in Humans
Cheng-Yung Lin, Hsiang-Yu Lin, Chih-Kuang Chuang, et al.
Journal of Personalized Medicine
|
July 27, 2022
Quantification of Idua Enzymatic Activity Combined with Observation of Phenotypic Change in Zebrafish Embryos Provide a Preliminary Assessment of Mutated <i>idua</i> Correlated with Mucopolysaccharidosis Type I
Cheng-Yung Lin, Hsiang-Yu Lin, Chih-Kuang Chuang, et al.
Journal of Personalized Medicine
|
July 27, 2022
Functional Independence of Taiwanese Children with Osteogenesis Imperfecta
Yu-Min Syu, Chung-Lin Lee, Chih-Kuang Chuang, et al.
Human Genetics
|
April 14, 2011
Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2
Hsiang-Yu Lin, Tina Jui-Ting Wu, Ju-Hui Hsu, et al.
Archives of Dermatological Research
|
April 7, 2007
Netherton syndrome: mutation analysis of two Taiwanese families
Shuan-Pei Lin, Shu-Yi Huang, Mei-Eng Tu, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
November 19, 2021
Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndrome
Chih-Ping Chen, Schu-Rern Chern, Chien-Hsing Lin, et al.
Journal of Clinical Ultrasound : JCU
|
March 22, 2007
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome
Chih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
April 29, 2008
Cri-du-chat syndrome
Chia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Page
of 19