Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S P Lin

Showing results (81-90 of 191) with videos related to

Pageof 20
Sort By:
Arthritis and Rheumatism|January 11, 2012
Quantitative imaging of cartilage and bone morphology, reactive oxygen species, and vascularization in a rodent model of osteoarthritisLiQin Xie, Angela S P Lin, Kousik Kundu, et al.
Genomics|March 1, 1992
Assignment of two human alpha-1,3-galactosyltransferase gene sequences (GGTA1 and GGTA1P) to chromosomes 9q33-q34 and 12q14-q15N L Shaper, S P Lin, D H Joziasse, et al.
Journal of Biomechanical Engineering|July 17, 2009
In vivo model for evaluating the effects of mechanical stimulation on tissue-engineered bone repairJoel D Boerckel, Kenneth M Dupont, Yash M Kolambkar, et al.
Clinical Genetics|March 1, 1995
Skipping of exon 12 as a consequence of a point mutation (1898 + 5G-->T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese familyJ Zielenski, D Markiewicz, S P Lin, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 2, 2002
Sonographic findings in a case of congenital pyloric diaphragmC P Chen, J C Sheu, S P Lin, et al.
Genetic Counseling (Geneva, Switzerland)|May 25, 2006
Recurrent Galloway Mowat syndrome associated with abnormal prenatal sonographic findingsC P Chen, S P Lin, T Y Chang, et al.
Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutationC-P Chen, S-P Lin, Y-N Su, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 1, 1988
Effects of prenatal exposure to neuroleptic drugs on children's growthJ E Platt, A J Friedhoff, S H Broman, et al.
The American Journal of Psychiatry|December 1, 1996
Schizoid personality disorder after prenatal exposure to famineH W Hoek, E Susser, K A Buck, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2012
Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndromeC P Chen, S P Lin, D S Lin, et al.
Pageof 20

Showing results (81-90 of 191) with videos related to

Sort By:
Pageof 20
Arthritis and Rheumatism|January 11, 2012
Quantitative imaging of cartilage and bone morphology, reactive oxygen species, and vascularization in a rodent model of osteoarthritisLiQin Xie, Angela S P Lin, Kousik Kundu, et al.
Genomics|March 1, 1992
Assignment of two human alpha-1,3-galactosyltransferase gene sequences (GGTA1 and GGTA1P) to chromosomes 9q33-q34 and 12q14-q15N L Shaper, S P Lin, D H Joziasse, et al.
Journal of Biomechanical Engineering|July 17, 2009
In vivo model for evaluating the effects of mechanical stimulation on tissue-engineered bone repairJoel D Boerckel, Kenneth M Dupont, Yash M Kolambkar, et al.
Clinical Genetics|March 1, 1995
Skipping of exon 12 as a consequence of a point mutation (1898 + 5G-->T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese familyJ Zielenski, D Markiewicz, S P Lin, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 2, 2002
Sonographic findings in a case of congenital pyloric diaphragmC P Chen, J C Sheu, S P Lin, et al.
Genetic Counseling (Geneva, Switzerland)|May 25, 2006
Recurrent Galloway Mowat syndrome associated with abnormal prenatal sonographic findingsC P Chen, S P Lin, T Y Chang, et al.
Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutationC-P Chen, S-P Lin, Y-N Su, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 1, 1988
Effects of prenatal exposure to neuroleptic drugs on children's growthJ E Platt, A J Friedhoff, S H Broman, et al.
The American Journal of Psychiatry|December 1, 1996
Schizoid personality disorder after prenatal exposure to famineH W Hoek, E Susser, K A Buck, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2012
Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndromeC P Chen, S P Lin, D S Lin, et al.
Pageof 20