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

J W Su

Showing results (11-20 of 23) with videos related to

Pageof 3
Sort By:
Genetic Counseling (Geneva, Switzerland)|October 18, 2012
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type IIIC P Chen, S P Lin, Y N Suo, et al.
The Thoracic and Cardiovascular Surgeon|August 4, 2010
Allograft entrapment after lung transplantation: a simple solution using a pleurocutaneous catheterN Vakil, J W Su, D P Mason, et al.
The Annals of Thoracic Surgery|October 4, 2000
Repair of cardiac defects through a shorter right lateral thoracotomy in childrenY L Liu, H J Zhang, H S Sun, 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.
Transplantation Proceedings|July 13, 2010
The effect of recipient hepatitis C virus infection on outcomes following heart transplantationA E Shafii, J W Su, N G Smedira, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Partial monosomy 9p (9p22.2-->pter) and partial trisomy 18q (18q21.32-->qter) in a female infant with anorectal malformationsC-P Chen, H-M Lin, C Leung, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactylyC-P Chen, S-P Lin, M-R Chen, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocationC-P Chen, S-P Lin, C-H Hsu, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delayC-P Chen, S-P Lin, Y-L Huang, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Genetic Counseling (Geneva, Switzerland)|October 18, 2012
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type IIIC P Chen, S P Lin, Y N Suo, et al.
The Thoracic and Cardiovascular Surgeon|August 4, 2010
Allograft entrapment after lung transplantation: a simple solution using a pleurocutaneous catheterN Vakil, J W Su, D P Mason, et al.
The Annals of Thoracic Surgery|October 4, 2000
Repair of cardiac defects through a shorter right lateral thoracotomy in childrenY L Liu, H J Zhang, H S Sun, 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.
Transplantation Proceedings|July 13, 2010
The effect of recipient hepatitis C virus infection on outcomes following heart transplantationA E Shafii, J W Su, N G Smedira, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Partial monosomy 9p (9p22.2-->pter) and partial trisomy 18q (18q21.32-->qter) in a female infant with anorectal malformationsC-P Chen, H-M Lin, C Leung, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactylyC-P Chen, S-P Lin, M-R Chen, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocationC-P Chen, S-P Lin, C-H Hsu, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delayC-P Chen, S-P Lin, Y-L Huang, et al.
Pageof 3