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Shuan-Pei Lin

Showing results (1-10 of 281) with videos related to

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Prenatal Diagnosis|November 27, 2004
Detection of chromosome aberrations during prenatal genetic testing for single gene disordersChih-Ping Chen, Shuan-Pei Lin
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: Osteogenesis imperfecta IIIHsiang-Yu Lin, Shuan-Pei Lin
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: OTC. Disease: ornithine transcarbamylase deficiencyHsiang-Yu Lin, Hsin-Yi Lin, Shuan-Pei Lin
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: osteogenesis imperfecta IVHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: osteogenesis imperfecta IVHsiang-Yu Lin, Chih-Kuang Chuang, Shuan-Pei Lin
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: osteogenesis imperfecta IVHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: osteogenesis imperfecta IHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang
Orphanet Journal of Rare Diseases|April 21, 2020
Assessing the impact of the five senses on quality of life in mucopolysaccharidosesRoberto Giugliani, Paul Harmatz, Shuan-Pei Lin, et al.
Prenatal Diagnosis|July 19, 2002
Microcephaly with dysgenesis of corpus callosum and colpocephaly in the survivor after the first-trimester death of a monochorionic co-twinChih-Ping Chen, Shuan-Pei Lin, Nan-Chang Chiu
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: osteogenesis imperfecta IHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang
Pageof 29

Showing results (1-10 of 281) with videos related to

Sort By:
Pageof 29
Prenatal Diagnosis|November 27, 2004
Detection of chromosome aberrations during prenatal genetic testing for single gene disordersChih-Ping Chen, Shuan-Pei Lin
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: Osteogenesis imperfecta IIIHsiang-Yu Lin, Shuan-Pei Lin
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: OTC. Disease: ornithine transcarbamylase deficiencyHsiang-Yu Lin, Hsin-Yi Lin, Shuan-Pei Lin
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: osteogenesis imperfecta IVHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: osteogenesis imperfecta IVHsiang-Yu Lin, Chih-Kuang Chuang, Shuan-Pei Lin
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: osteogenesis imperfecta IVHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: osteogenesis imperfecta IHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang
Orphanet Journal of Rare Diseases|April 21, 2020
Assessing the impact of the five senses on quality of life in mucopolysaccharidosesRoberto Giugliani, Paul Harmatz, Shuan-Pei Lin, et al.
Prenatal Diagnosis|July 19, 2002
Microcephaly with dysgenesis of corpus callosum and colpocephaly in the survivor after the first-trimester death of a monochorionic co-twinChih-Ping Chen, Shuan-Pei Lin, Nan-Chang Chiu
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: COL1A2. Disease: osteogenesis imperfecta IHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang
Pageof 29