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American Journal of Translational Research
|
December 23, 2015
Targeted next-generation sequencing of cancer genes identified frequent TP53 and ATRX mutations in leiomyosarcoma
Ching-Yao Yang, Jau-Yu Liau, Wei-Ju Huang, et al.
Electrophoresis
|
January 18, 2008
Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: a comparison
Chia-Cheng Hung, Chien-Nan Lee, Chia-Yun Lin, et al.
Electrophoresis
|
January 13, 2009
Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR
Chia-Cheng Hung, Shin-Yu Lin, Shuan-Pei Lin, et al.
Plos One
|
March 3, 2011
Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: a prospective population-based cohort study
Yi-Ning Su, Chia-Cheng Hung, Shin-Yu Lin, et al.
Scientific Reports
|
October 31, 2019
Fragile X syndrome carrier screening in pregnant women in Chinese Han population
Chia-Cheng Hung, Chien-Nan Lee, Yu-Chu Wang, et al.
Human Mutation
|
April 16, 2005
Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a highly efficient and reliable carrier-screening test
Yi-Ning Su, Chia-Cheng Hung, Hung Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 17, 2016
Newborn genetic screening for hearing impairment: a population-based longitudinal study
Chen-Chi Wu, Ching-Hui Tsai, Chia-Cheng Hung, et al.
BMC Medical Genetics
|
September 20, 2006
Molecular and clinical analyses of 84 patients with tuberous sclerosis complex
Chia-Cheng Hung, Yi-Ning Su, Shu-Chin Chien, et al.
Clinical and Experimental Otorhinolaryngology
|
February 13, 2025
Screening for Hearing Impairment in Newborns Using Targeted Genomic Sequencing: A Large Pilot Cohort Study
Pei-Hsuan Lin, Yu-Ting Chiang, Cheng-Yu Tsai, et al.
Electrophoresis
|
February 16, 2007
Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE
Chia-Cheng Hung, Yi-Ning Su, Po-Nien Tsao, et al.
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Showing results (31-40 of 48) with videos related to
Sort By:
Page
of 5
American Journal of Translational Research
|
December 23, 2015
Targeted next-generation sequencing of cancer genes identified frequent TP53 and ATRX mutations in leiomyosarcoma
Ching-Yao Yang, Jau-Yu Liau, Wei-Ju Huang, et al.
Electrophoresis
|
January 18, 2008
Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: a comparison
Chia-Cheng Hung, Chien-Nan Lee, Chia-Yun Lin, et al.
Electrophoresis
|
January 13, 2009
Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR
Chia-Cheng Hung, Shin-Yu Lin, Shuan-Pei Lin, et al.
Plos One
|
March 3, 2011
Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: a prospective population-based cohort study
Yi-Ning Su, Chia-Cheng Hung, Shin-Yu Lin, et al.
Scientific Reports
|
October 31, 2019
Fragile X syndrome carrier screening in pregnant women in Chinese Han population
Chia-Cheng Hung, Chien-Nan Lee, Yu-Chu Wang, et al.
Human Mutation
|
April 16, 2005
Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a highly efficient and reliable carrier-screening test
Yi-Ning Su, Chia-Cheng Hung, Hung Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 17, 2016
Newborn genetic screening for hearing impairment: a population-based longitudinal study
Chen-Chi Wu, Ching-Hui Tsai, Chia-Cheng Hung, et al.
BMC Medical Genetics
|
September 20, 2006
Molecular and clinical analyses of 84 patients with tuberous sclerosis complex
Chia-Cheng Hung, Yi-Ning Su, Shu-Chin Chien, et al.
Clinical and Experimental Otorhinolaryngology
|
February 13, 2025
Screening for Hearing Impairment in Newborns Using Targeted Genomic Sequencing: A Large Pilot Cohort Study
Pei-Hsuan Lin, Yu-Ting Chiang, Cheng-Yu Tsai, et al.
Electrophoresis
|
February 16, 2007
Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE
Chia-Cheng Hung, Yi-Ning Su, Po-Nien Tsao, et al.
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of 5