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

A Kariminejad

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
Clinical and Experimental Dermatology|April 25, 2014
Olmsted syndrome in an Iranian boy with a new de novo mutation in TRPV3A Kariminejad, M Barzegar, F Abdollahimajd, et al.
The British Journal of Dermatology|July 23, 2013
A new homozygous nonsense mutation in LAMA3A underlying laryngo-onycho-cutaneous syndromeM Barzegar, N Mozafari, A Kariminejad, et al.
Clinical Genetics|June 13, 2012
Mutation analysis of the STRA6 gene in isolated and non-isolated anophthalmia/microphthalmiaN Chassaing, N Ragge, A Kariminejad, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 14, 2016
CYP2U1 mutations in two Iranian patients with activity induced dystonia, motor regression and spastic paraplegiaA Kariminejad, L Schöls, R Schüle, et al.
Molecular Syndromology|May 10, 2012
Osteogenesis Imperfecta: A Review with Clinical ExamplesF S van Dijk, J M Cobben, A Kariminejad, et al.
Clinical Genetics|May 29, 2016
Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous populationZ Fattahi, Z Kalhor, M Fadaee, et al.
Diabetologia|June 5, 2012
SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretionF H Sansbury, S E Flanagan, J A L Houghton, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Clinical and Experimental Dermatology|April 25, 2014
Olmsted syndrome in an Iranian boy with a new de novo mutation in TRPV3A Kariminejad, M Barzegar, F Abdollahimajd, et al.
The British Journal of Dermatology|July 23, 2013
A new homozygous nonsense mutation in LAMA3A underlying laryngo-onycho-cutaneous syndromeM Barzegar, N Mozafari, A Kariminejad, et al.
Clinical Genetics|June 13, 2012
Mutation analysis of the STRA6 gene in isolated and non-isolated anophthalmia/microphthalmiaN Chassaing, N Ragge, A Kariminejad, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 14, 2016
CYP2U1 mutations in two Iranian patients with activity induced dystonia, motor regression and spastic paraplegiaA Kariminejad, L Schöls, R Schüle, et al.
Molecular Syndromology|May 10, 2012
Osteogenesis Imperfecta: A Review with Clinical ExamplesF S van Dijk, J M Cobben, A Kariminejad, et al.
Clinical Genetics|May 29, 2016
Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous populationZ Fattahi, Z Kalhor, M Fadaee, et al.
Diabetologia|June 5, 2012
SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretionF H Sansbury, S E Flanagan, J A L Houghton, et al.
Pageof 1