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

W Ahmad

Showing results (71-80 of 193) with videos related to

Pageof 20
Sort By:
The British Journal of Dermatology|July 8, 2015
Genetics of human isolated hereditary nail disordersS Khan, S Basit, R Habib, et al.
Journal of Applied Genetics|May 13, 2009
High-quality plant DNA extraction for PCR: an easy approachI Ahmed, M Islam, W Arshad, et al.
Clinical Genetics|June 10, 2010
Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigreesS Basit, A Wali, A Aziz, et al.
Clinical and Experimental Dermatology|July 20, 2019
Woodhouse-Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 geneK Shah, A Jan, F Ahmad, et al.
The Journal of Investigative Dermatology|September 1, 1999
A homozygous nonsense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichiaW Ahmad, K Nomura, J A McGrath, et al.
The British Journal of Dermatology|June 4, 2010
Mapping of a novel locus for an autosomal recessive form of palmoplantar keratoderma on chromosome 3q27.2-q29S Khan, S Muzaffar, M Tariq, et al.
The British Journal of Dermatology|December 12, 2007
A novel missense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a consanguineous Pakistani familyM S Chishti, N Kausar, M A Rafiq, et al.
Clinical Genetics|October 13, 2017
First direct evidence of involvement of a homozygous loss-of-function variant in the EPS15L1 gene underlying split-hand/split-foot malformationM Umair, A Ullah, S Abbas, et al.
The American Surgeon|April 1, 1982
Applications of choledochoduodenostomy in biliary tract obstructionD E Fry, E Buchignani, H C Polk, et al.
Experimental Dermatology|December 1, 1998
Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humansA A Panteleyev, R Paus, W Ahmad, et al.
Pageof 20

Showing results (71-80 of 193) with videos related to

Sort By:
Pageof 20
The British Journal of Dermatology|July 8, 2015
Genetics of human isolated hereditary nail disordersS Khan, S Basit, R Habib, et al.
Journal of Applied Genetics|May 13, 2009
High-quality plant DNA extraction for PCR: an easy approachI Ahmed, M Islam, W Arshad, et al.
Clinical Genetics|June 10, 2010
Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigreesS Basit, A Wali, A Aziz, et al.
Clinical and Experimental Dermatology|July 20, 2019
Woodhouse-Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 geneK Shah, A Jan, F Ahmad, et al.
The Journal of Investigative Dermatology|September 1, 1999
A homozygous nonsense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichiaW Ahmad, K Nomura, J A McGrath, et al.
The British Journal of Dermatology|June 4, 2010
Mapping of a novel locus for an autosomal recessive form of palmoplantar keratoderma on chromosome 3q27.2-q29S Khan, S Muzaffar, M Tariq, et al.
The British Journal of Dermatology|December 12, 2007
A novel missense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a consanguineous Pakistani familyM S Chishti, N Kausar, M A Rafiq, et al.
Clinical Genetics|October 13, 2017
First direct evidence of involvement of a homozygous loss-of-function variant in the EPS15L1 gene underlying split-hand/split-foot malformationM Umair, A Ullah, S Abbas, et al.
The American Surgeon|April 1, 1982
Applications of choledochoduodenostomy in biliary tract obstructionD E Fry, E Buchignani, H C Polk, et al.
Experimental Dermatology|December 1, 1998
Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humansA A Panteleyev, R Paus, W Ahmad, et al.
Pageof 20