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

T R Wang

Showing results (11-20 of 157) with videos related to

Pageof 16
Sort By:
Journal of the Formosan Medical Association = Taiwan Yi Zhi|February 1, 1996
Amino acid and DNA analyses in a family with ornithine transcarbamylase deficiencyJ W Hou, T R Wang
American Journal of Medical Genetics|August 28, 1995
Clinical variability in neonatal progeroid syndromeJ W Hou, T R Wang
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|March 1, 1997
Differentiation of Fanconi anemia from aplastic anemia by chromosomal breakage testJ W Hou, T R Wang
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|September 1, 1991
Quantification of arylsulfatase B activity and diagnosis of Maroteaux-Lamy syndromeW L Hwu, T R Wang
American Journal of Medical Genetics|October 1, 1987
Further evidence for genetic heterogeneity of whistling face or Freeman-Sheldon syndrome in a Chinese familyT R Wang, S J Lin
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000
Study of human Y chromosome polymorphism in TaiwanJ W Hou, T R Wang
American Journal of Medical Genetics|September 11, 1995
Galloway-Mowat syndrome in TaiwanJ W Hou, T R Wang
Journal of Medical Genetics|October 1, 1996
Amelia, dextrocardia, asplenia, and congenital short bowel in deleted ring chromosome 4J W Hou, T R Wang
European Journal of Pediatrics|May 20, 1999
Extreme Poland anomaly associated with congenital diaphragmatic herniaJ W Hou, T R Wang
Journal of the Formosan Medical Association = Taiwan Yi Zhi|January 1, 1997
Primed in situ (PRINS) labeling for rapid detection of numeric and structural chromosome anomaliesJ W Hou, T R Wang
Pageof 16

Showing results (11-20 of 157) with videos related to

Sort By:
Pageof 16
Journal of the Formosan Medical Association = Taiwan Yi Zhi|February 1, 1996
Amino acid and DNA analyses in a family with ornithine transcarbamylase deficiencyJ W Hou, T R Wang
American Journal of Medical Genetics|August 28, 1995
Clinical variability in neonatal progeroid syndromeJ W Hou, T R Wang
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|March 1, 1997
Differentiation of Fanconi anemia from aplastic anemia by chromosomal breakage testJ W Hou, T R Wang
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|September 1, 1991
Quantification of arylsulfatase B activity and diagnosis of Maroteaux-Lamy syndromeW L Hwu, T R Wang
American Journal of Medical Genetics|October 1, 1987
Further evidence for genetic heterogeneity of whistling face or Freeman-Sheldon syndrome in a Chinese familyT R Wang, S J Lin
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000
Study of human Y chromosome polymorphism in TaiwanJ W Hou, T R Wang
American Journal of Medical Genetics|September 11, 1995
Galloway-Mowat syndrome in TaiwanJ W Hou, T R Wang
Journal of Medical Genetics|October 1, 1996
Amelia, dextrocardia, asplenia, and congenital short bowel in deleted ring chromosome 4J W Hou, T R Wang
European Journal of Pediatrics|May 20, 1999
Extreme Poland anomaly associated with congenital diaphragmatic herniaJ W Hou, T R Wang
Journal of the Formosan Medical Association = Taiwan Yi Zhi|January 1, 1997
Primed in situ (PRINS) labeling for rapid detection of numeric and structural chromosome anomaliesJ W Hou, T R Wang
Pageof 16