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Wei-De Lin

Showing results (1-10 of 93) with videos related to

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Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: EXT1. Disease: multiple exostosesWei-De Lin, Fuu-Jer Tsai
Biomedicine Hub|January 27, 2022
Genetic Analysis of Acid β-Glucosidase in Patients with Multiple Myeloma from Central Taiwan: A Small-Cohort Case-Control StudyWei-De Lin, Fuu-Jen Tsai
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plusI Ching Chou, Wei-De Lin, Fuu-Jen Tsai
Pediatrics and Neonatology|November 12, 2019
Mild osteochondrodysplasia with acanthosis nigricans in a short-statured Taiwanese family due to the p.Lys650Gln mutation in FGFR3Wei-De Lin, Fuu-Jen Tsai, Chung-Hsing Wang
Pediatrics and Neonatology|March 6, 2018
Identification of one novel homozygous mutation in the NPR2 gene in a patient from Taiwan with acromesomelic dysplasia Maroteaux typeWei-De Lin, Chung-Hsing Wang, Fuu-Jen Tsai
Biomedical Journal|January 18, 2022
Current understanding of the genetics of tourette syndromeWei-De Lin, Fuu-Jen Tsai, I-Ching Chou
Pediatrics and Neonatology|June 6, 2023
Identification of a novel deletion mutation in PHKA2 in a taiwanese patient with type IXa glycogen storage diseaseWei-De Lin, Fuu-Jen Tsai, Chung-Hsing Wang
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plusWei-De Lin, I Ching Chou, Fuu-Jen Tsai
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plusI Ching Chou, Wei-De Lin, Fuu-Jen Tsai
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plusWei-De Lin, I-Ching Chou, Fuu-Jen Tsai
Pageof 10

Showing results (1-10 of 93) with videos related to

Sort By:
Pageof 10
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: EXT1. Disease: multiple exostosesWei-De Lin, Fuu-Jer Tsai
Biomedicine Hub|January 27, 2022
Genetic Analysis of Acid β-Glucosidase in Patients with Multiple Myeloma from Central Taiwan: A Small-Cohort Case-Control StudyWei-De Lin, Fuu-Jen Tsai
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plusI Ching Chou, Wei-De Lin, Fuu-Jen Tsai
Pediatrics and Neonatology|November 12, 2019
Mild osteochondrodysplasia with acanthosis nigricans in a short-statured Taiwanese family due to the p.Lys650Gln mutation in FGFR3Wei-De Lin, Fuu-Jen Tsai, Chung-Hsing Wang
Pediatrics and Neonatology|March 6, 2018
Identification of one novel homozygous mutation in the NPR2 gene in a patient from Taiwan with acromesomelic dysplasia Maroteaux typeWei-De Lin, Chung-Hsing Wang, Fuu-Jen Tsai
Biomedical Journal|January 18, 2022
Current understanding of the genetics of tourette syndromeWei-De Lin, Fuu-Jen Tsai, I-Ching Chou
Pediatrics and Neonatology|June 6, 2023
Identification of a novel deletion mutation in PHKA2 in a taiwanese patient with type IXa glycogen storage diseaseWei-De Lin, Fuu-Jen Tsai, Chung-Hsing Wang
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plusWei-De Lin, I Ching Chou, Fuu-Jen Tsai
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plusI Ching Chou, Wei-De Lin, Fuu-Jen Tsai
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plusWei-De Lin, I-Ching Chou, Fuu-Jen Tsai
Pageof 10