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Chia-Cheng Hung

Showing results (41-50 of 48) with videos related to

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Electrophoresis|July 21, 2007
Use of multiplex PCR and CE for gene dosage quantification and its biomedical applications for SMN, PMP22, and alpha-globin genesChia-Cheng Hung, Shu-Chin Chien, Chia-Yun Lin, et al.
The Journal of Pediatrics|April 24, 2018
Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, TaiwanChun-Yi Lu, Po-Nien Tsao, Ying-Ying Ke, et al.
Analytical Biochemistry|March 31, 2009
Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysisChia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, et al.
Annals of Human Genetics|October 21, 2009
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndromeChia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, et al.
Cancer Science|November 16, 2019
TP53 alterations in relapsed childhood acute lymphoblastic leukemiaChih-Hsiang Yu, Wan-Ting Chang, Shiann-Tarng Jou, et al.
American Journal of Medical Genetics. Part A|September 11, 2010
Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndromeShin-Yu Lin, Chien-Nan Lee, Chia-Cheng Hung, et al.
Cancer Science|July 12, 2011
IKZF1 deletions predict a poor prognosis in children with B-cell progenitor acute lymphoblastic leukemia: a multicenter analysis in TaiwanYung-Li Yang, Chia-Cheng Hung, Jiann-Shiuh Chen, et al.
Scientific Reports|July 15, 2020
MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemiaChih-Hsiang Yu, Tze-Kang Lin, Shiann-Tarng Jou, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Electrophoresis|July 21, 2007
Use of multiplex PCR and CE for gene dosage quantification and its biomedical applications for SMN, PMP22, and alpha-globin genesChia-Cheng Hung, Shu-Chin Chien, Chia-Yun Lin, et al.
The Journal of Pediatrics|April 24, 2018
Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, TaiwanChun-Yi Lu, Po-Nien Tsao, Ying-Ying Ke, et al.
Analytical Biochemistry|March 31, 2009
Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysisChia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, et al.
Annals of Human Genetics|October 21, 2009
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndromeChia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, et al.
Cancer Science|November 16, 2019
TP53 alterations in relapsed childhood acute lymphoblastic leukemiaChih-Hsiang Yu, Wan-Ting Chang, Shiann-Tarng Jou, et al.
American Journal of Medical Genetics. Part A|September 11, 2010
Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndromeShin-Yu Lin, Chien-Nan Lee, Chia-Cheng Hung, et al.
Cancer Science|July 12, 2011
IKZF1 deletions predict a poor prognosis in children with B-cell progenitor acute lymphoblastic leukemia: a multicenter analysis in TaiwanYung-Li Yang, Chia-Cheng Hung, Jiann-Shiuh Chen, et al.
Scientific Reports|July 15, 2020
MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemiaChih-Hsiang Yu, Tze-Kang Lin, Shiann-Tarng Jou, et al.
Pageof 5