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Shuan-Pei Lin

Showing results (21-30 of 281) with videos related to

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Acta Cardiologica|March 23, 2005
Cardiovascular changes in mucopolysaccharidoses in TaiwanMing-Ren Chen, Shuan-Pei Lin, Haw-Kwei Hwang, et al.
Human Genetics|April 4, 2008
Human gene mutations. Gene symbol: EXT1. Disease: exostoses (multiple) 1Wei-De Lin, Shuan-Pei Lin, Chih-Ping Chen, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|July 11, 2014
Mucopolysaccharidosis I (Scheie syndrome): A rare cause of severe aortic stenosis in a 31-year-old manHsiang-Yu Lin, Chi-In Lo, Chih-Kuang Chuang, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
Generalized arterial calcification of infancy: different clinical courses in two affected siblingsKun-Shan Cheng, Ming-Ren Chen, Nico Ruf, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 28, 2007
Characterization of a novel p.S305P and a known c.1006+5G>C splice site mutation in human iduronate-2-sulfatase associated with mucopolysaccharidosis type IIJui-Hung Chang, Guey-Jen Lee-Chen, Shuan-Pei Lin, et al.
Prenatal Diagnosis|May 3, 2006
Prenatal sonography and magnetic resonance imaging of pulmonary sequestration associated with a gastric duplication cystChih-Ping Chen, Yu-Peng Liu, Chin-Yuan Hsu, et al.
Prenatal Diagnosis|February 14, 2006
Neonatal outcome of a prenatally detected 46,XX/46,XY true hermaphroditeChih-Ping Chen, Shuan-Pei Lin, Jin-Chern Sheu, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 19, 2015
Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening resultChih-Ping Chen, Shuan-Pei Lin, Hui-Bo Li, et al.
Prenatal Diagnosis|May 28, 2004
Second-trimester nasal bone hypoplasia/aplasia associated with cleidocranial dysplasiaChih-Ping Chen, Han-Yang Hung, Tung-Yao Chang, et al.
Prenatal Diagnosis|February 14, 2006
Favourable outcome in a pregnancy with concomitant maternal and fetal osteogenesis imperfecta associated with a novel COL1A2 mutationChih-Ping Chen, Yi-Ning Su, Shuan-Pei Lin, et al.
Pageof 29

Showing results (21-30 of 281) with videos related to

Sort By:
Pageof 29
Acta Cardiologica|March 23, 2005
Cardiovascular changes in mucopolysaccharidoses in TaiwanMing-Ren Chen, Shuan-Pei Lin, Haw-Kwei Hwang, et al.
Human Genetics|April 4, 2008
Human gene mutations. Gene symbol: EXT1. Disease: exostoses (multiple) 1Wei-De Lin, Shuan-Pei Lin, Chih-Ping Chen, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|July 11, 2014
Mucopolysaccharidosis I (Scheie syndrome): A rare cause of severe aortic stenosis in a 31-year-old manHsiang-Yu Lin, Chi-In Lo, Chih-Kuang Chuang, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
Generalized arterial calcification of infancy: different clinical courses in two affected siblingsKun-Shan Cheng, Ming-Ren Chen, Nico Ruf, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 28, 2007
Characterization of a novel p.S305P and a known c.1006+5G>C splice site mutation in human iduronate-2-sulfatase associated with mucopolysaccharidosis type IIJui-Hung Chang, Guey-Jen Lee-Chen, Shuan-Pei Lin, et al.
Prenatal Diagnosis|May 3, 2006
Prenatal sonography and magnetic resonance imaging of pulmonary sequestration associated with a gastric duplication cystChih-Ping Chen, Yu-Peng Liu, Chin-Yuan Hsu, et al.
Prenatal Diagnosis|February 14, 2006
Neonatal outcome of a prenatally detected 46,XX/46,XY true hermaphroditeChih-Ping Chen, Shuan-Pei Lin, Jin-Chern Sheu, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 19, 2015
Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening resultChih-Ping Chen, Shuan-Pei Lin, Hui-Bo Li, et al.
Prenatal Diagnosis|May 28, 2004
Second-trimester nasal bone hypoplasia/aplasia associated with cleidocranial dysplasiaChih-Ping Chen, Han-Yang Hung, Tung-Yao Chang, et al.
Prenatal Diagnosis|February 14, 2006
Favourable outcome in a pregnancy with concomitant maternal and fetal osteogenesis imperfecta associated with a novel COL1A2 mutationChih-Ping Chen, Yi-Ning Su, Shuan-Pei Lin, et al.
Pageof 29