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

G Al Thani

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
Annals of Tropical Paediatrics|November 7, 2000
Cystic fibrosis in a large kindred family in QatarA Abdul Wahab, S T Dawod, G al Thani
Journal of Tropical Pediatrics|April 20, 2004
Rare CFTR mutation 1525-1G>A in a Pakistani patientAbdul Wahab, G Al Thani, S T Dawod, et al.
Journal of Tropical Pediatrics|May 5, 2001
Heterogeneity of the cystic fibrosis phenotype in a large kindred family in Qatar with cystic fibrosis mutation (I1234V)A Abdul Wahab, G Al Thani, S T Dawod, et al.
Clinical Genetics|June 21, 2008
Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari familiesM Faiyaz-Ul-Haque, S H E Zaidi, A A Wahab, et al.
Journal of Inherited Metabolic Disease|May 19, 2007
Implementation of extended neonatal screening and a metabolic unit in the State of Qatar: developing and optimizing strategies in cooperation with the Neonatal Screening Center in HeidelbergM Lindner, G Abdoh, J Fang-Hoffmann, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Annals of Tropical Paediatrics|November 7, 2000
Cystic fibrosis in a large kindred family in QatarA Abdul Wahab, S T Dawod, G al Thani
Journal of Tropical Pediatrics|April 20, 2004
Rare CFTR mutation 1525-1G>A in a Pakistani patientAbdul Wahab, G Al Thani, S T Dawod, et al.
Journal of Tropical Pediatrics|May 5, 2001
Heterogeneity of the cystic fibrosis phenotype in a large kindred family in Qatar with cystic fibrosis mutation (I1234V)A Abdul Wahab, G Al Thani, S T Dawod, et al.
Clinical Genetics|June 21, 2008
Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari familiesM Faiyaz-Ul-Haque, S H E Zaidi, A A Wahab, et al.
Journal of Inherited Metabolic Disease|May 19, 2007
Implementation of extended neonatal screening and a metabolic unit in the State of Qatar: developing and optimizing strategies in cooperation with the Neonatal Screening Center in HeidelbergM Lindner, G Abdoh, J Fang-Hoffmann, et al.
Pageof 1