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Shuan-Pei Lin

Showing results (101-110 of 281) with videos related to

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Archives of Dermatological Research|April 7, 2007
Netherton syndrome: mutation analysis of two Taiwanese familiesShuan-Pei Lin, Shu-Yi Huang, Mei-Eng Tu, et al.
Human Genetics|December 23, 2004
Expression studies of mutations underlying Taiwanese Hunter syndrome (mucopolysaccharidosis type II)Jui-Hung Chang, Shuan-Pei Lin, Shu-Chuan Lin, et al.
Prenatal Diagnosis|October 16, 2002
Perinatal imaging findings of inherited Sotos syndromeChih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 4, 2013
Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistryChih-Ping Chen, Yi-Ning Su, Shuan-Pei Lin, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|April 29, 2008
Cri-du-chat syndromeChia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 4, 2017
Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delayChih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 21, 2018
A 17-year-old boy with Klinefelter syndrome presenting Marfan syndrome-like clinical features of tall stature, scoliosis, arachnodactyly and subluxation of bilateral elbow jointsChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 4, 2017
Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorderChih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, et al.
Prenatal Diagnosis|July 29, 2005
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2-->qter) and partial monosomy 5p (5p15.3-->pter)Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, et al.
Journal of Clinical Ultrasound : JCU|March 22, 2007
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndromeChih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, et al.
Pageof 29

Showing results (101-110 of 281) with videos related to

Sort By:
Pageof 29
Archives of Dermatological Research|April 7, 2007
Netherton syndrome: mutation analysis of two Taiwanese familiesShuan-Pei Lin, Shu-Yi Huang, Mei-Eng Tu, et al.
Human Genetics|December 23, 2004
Expression studies of mutations underlying Taiwanese Hunter syndrome (mucopolysaccharidosis type II)Jui-Hung Chang, Shuan-Pei Lin, Shu-Chuan Lin, et al.
Prenatal Diagnosis|October 16, 2002
Perinatal imaging findings of inherited Sotos syndromeChih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 4, 2013
Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistryChih-Ping Chen, Yi-Ning Su, Shuan-Pei Lin, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|April 29, 2008
Cri-du-chat syndromeChia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 4, 2017
Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delayChih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 21, 2018
A 17-year-old boy with Klinefelter syndrome presenting Marfan syndrome-like clinical features of tall stature, scoliosis, arachnodactyly and subluxation of bilateral elbow jointsChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 4, 2017
Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorderChih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, et al.
Prenatal Diagnosis|July 29, 2005
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2-->qter) and partial monosomy 5p (5p15.3-->pter)Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, et al.
Journal of Clinical Ultrasound : JCU|March 22, 2007
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndromeChih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, et al.
Pageof 29