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Wei-De Lin

Showing results (31-40 of 93) with videos related to

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Biotechnology Progress|April 2, 2005
Asymmetrical synthesis of L-homophenylalanine using engineered Escherichia coli aspartate aminotransferaseHsueh-Hsia Lo, Shih-Kuang Hsu, Wei-De Lin, et al.
Human Genetics|April 4, 2008
Human gene mutations. Gene symbol: GLA. Disease: Fabry diseaseWei-De Lin, Wuh-Liang Hwu, Su-Chiang Liu, et al.
BMC Pediatrics|November 6, 2019
Heterogeneous neurodevelopmental disorders in children with Kawasaki disease: what is new today?Chien-Heng Lin, Wei-De Lin, I-Ching Chou, et al.
The Tohoku Journal of Experimental Medicine|March 24, 2015
Deletion of exon 4 in the N-acetylgalactosamine-4-sulfatase gene in a Taiwanese patient with mucopolysaccharidosis type VIWei-De Lin, Yu-Yuan Ke, I-Ching Chou, et al.
Chromosoma|August 2, 2014
Characterization of maize B-chromosome-related transcripts isolated via cDNA-AFLPHuan-Zhi Lin, Wei-De Lin, Chien-Yu Lin, et al.
Human Genetics|October 21, 2010
Gene symbol: GCDH. Disease: Glutaricacidaemia IWei-De Lin, Wuh-Liang Hwu, Chung-Hsing Wang, et al.
Life (Basel, Switzerland)|August 27, 2021
Is Preterm Birth a Risk Factor for Subsequent Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder in Children with Febrile Seizure?-A Retrospective StudyChien-Heng Lin, Wei-De Lin, I-Ching Chou, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 3, 2011
Association study in Taiwanese girls with precocious pubertyI-Ching Chou, Chung-Hsing Wang, Wei-De Lin, et al.
Pediatrics and Neonatology|September 15, 2015
Identification and Characterization of Mutations in the CLCN7 Gene in a Taiwanese Patient with Infantile Malignant OsteopetrosisWei-De Lin, Chung-Hsing Wang, Kang-His Wu, et al.
Frontiers in Neurology|June 4, 2019
Epilepsy and Neurodevelopmental Outcomes in Children With Etiologically Diagnosed Central Nervous System Infections: A Retrospective Cohort StudyChien-Heng Lin, Wei-De Lin, I-Ching Chou, et al.
Pageof 10

Showing results (31-40 of 93) with videos related to

Sort By:
Pageof 10
Biotechnology Progress|April 2, 2005
Asymmetrical synthesis of L-homophenylalanine using engineered Escherichia coli aspartate aminotransferaseHsueh-Hsia Lo, Shih-Kuang Hsu, Wei-De Lin, et al.
Human Genetics|April 4, 2008
Human gene mutations. Gene symbol: GLA. Disease: Fabry diseaseWei-De Lin, Wuh-Liang Hwu, Su-Chiang Liu, et al.
BMC Pediatrics|November 6, 2019
Heterogeneous neurodevelopmental disorders in children with Kawasaki disease: what is new today?Chien-Heng Lin, Wei-De Lin, I-Ching Chou, et al.
The Tohoku Journal of Experimental Medicine|March 24, 2015
Deletion of exon 4 in the N-acetylgalactosamine-4-sulfatase gene in a Taiwanese patient with mucopolysaccharidosis type VIWei-De Lin, Yu-Yuan Ke, I-Ching Chou, et al.
Chromosoma|August 2, 2014
Characterization of maize B-chromosome-related transcripts isolated via cDNA-AFLPHuan-Zhi Lin, Wei-De Lin, Chien-Yu Lin, et al.
Human Genetics|October 21, 2010
Gene symbol: GCDH. Disease: Glutaricacidaemia IWei-De Lin, Wuh-Liang Hwu, Chung-Hsing Wang, et al.
Life (Basel, Switzerland)|August 27, 2021
Is Preterm Birth a Risk Factor for Subsequent Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder in Children with Febrile Seizure?-A Retrospective StudyChien-Heng Lin, Wei-De Lin, I-Ching Chou, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 3, 2011
Association study in Taiwanese girls with precocious pubertyI-Ching Chou, Chung-Hsing Wang, Wei-De Lin, et al.
Pediatrics and Neonatology|September 15, 2015
Identification and Characterization of Mutations in the CLCN7 Gene in a Taiwanese Patient with Infantile Malignant OsteopetrosisWei-De Lin, Chung-Hsing Wang, Kang-His Wu, et al.
Frontiers in Neurology|June 4, 2019
Epilepsy and Neurodevelopmental Outcomes in Children With Etiologically Diagnosed Central Nervous System Infections: A Retrospective Cohort StudyChien-Heng Lin, Wei-De Lin, I-Ching Chou, et al.
Pageof 10