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S P Lin

Showing results (111-120 of 191) with videos related to

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Genetic Counseling (Geneva, Switzerland)|May 25, 2006
Molecular cytogenetic analysis of de novo partial monosomy 4p (4p16.2-->pter) and partial trisomy 8p (8p23.2-->pter)C P Chen, S P Lin, S R Chern, et al.
British Journal of Anaesthesia|December 14, 2011
Discriminant analysis for anaesthetic decision-making: an intelligent recognition system for epidural needle insertionS P Lin, M S Mandell, Y Chang, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delayC P Chen, S P Lin, S R Chern, et al.
Clinical Nephrology|May 25, 2005
7-84 parathyroid hormone fragments are proportionally increased with the severity of uremic hyperparathyroidismJ M Chang, S P Lin, H T Kuo, et al.
Biomaterials|September 22, 2018
Porous PEEK improves the bone-implant interface compared to plasma-sprayed titanium coating on PEEKF Brennan Torstrick, Angela S P Lin, Daniel Potter, et al.
Genetic Counseling (Geneva, Switzerland)|February 7, 2012
Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disabilityC-P Chen, S-P Lin, S-R Chern, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delayC-P Chen, S-P Lin, Y-N Su, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Pure distal 9p deletion in a female infant with cerebral palsyC-P Chen, S-P Lin, Y-N Su, et al.
Zhonghua Yi Xue Za Zhi|December 1, 2020
[Clinical characteristics and related factors of acute tubular necrosis in patients with minimal change disease]S P Lin, J L Meng, X W Sun, et al.
Genetic Counseling (Geneva, Switzerland)|October 28, 2011
Self-injurious behavior associated with trisomy 9p (9p13.1 --> p24.3)C P Chen, S P Lin, Y N Su, et al.
Pageof 20

Showing results (111-120 of 191) with videos related to

Sort By:
Pageof 20
Genetic Counseling (Geneva, Switzerland)|May 25, 2006
Molecular cytogenetic analysis of de novo partial monosomy 4p (4p16.2-->pter) and partial trisomy 8p (8p23.2-->pter)C P Chen, S P Lin, S R Chern, et al.
British Journal of Anaesthesia|December 14, 2011
Discriminant analysis for anaesthetic decision-making: an intelligent recognition system for epidural needle insertionS P Lin, M S Mandell, Y Chang, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delayC P Chen, S P Lin, S R Chern, et al.
Clinical Nephrology|May 25, 2005
7-84 parathyroid hormone fragments are proportionally increased with the severity of uremic hyperparathyroidismJ M Chang, S P Lin, H T Kuo, et al.
Biomaterials|September 22, 2018
Porous PEEK improves the bone-implant interface compared to plasma-sprayed titanium coating on PEEKF Brennan Torstrick, Angela S P Lin, Daniel Potter, et al.
Genetic Counseling (Geneva, Switzerland)|February 7, 2012
Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disabilityC-P Chen, S-P Lin, S-R Chern, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delayC-P Chen, S-P Lin, Y-N Su, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Pure distal 9p deletion in a female infant with cerebral palsyC-P Chen, S-P Lin, Y-N Su, et al.
Zhonghua Yi Xue Za Zhi|December 1, 2020
[Clinical characteristics and related factors of acute tubular necrosis in patients with minimal change disease]S P Lin, J L Meng, X W Sun, et al.
Genetic Counseling (Geneva, Switzerland)|October 28, 2011
Self-injurious behavior associated with trisomy 9p (9p13.1 --> p24.3)C P Chen, S P Lin, Y N Su, et al.
Pageof 20