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

Elon Pras

Showing results (31-40 of 103) with videos related to

Pageof 11
Sort By:
American Journal of Human Genetics|May 3, 2008
Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndromeAlmogit Abu, Moshe Frydman, Dina Marek, et al.
The Israel Medical Association Journal : IMAJ|June 26, 2017
Colorectal and Endometrial Cancer Risk and Age at Diagnosis in BLMAsh Mutation CarriersHagit Schayek, Yael Laitman, Lior H Katz, et al.
Seminars in Arthritis and Rheumatism|January 17, 2012
NOD2/CARD15 gene mutations in patients with familial Mediterranean feverYackov Berkun, Amir Karban, Shai Padeh, et al.
Molecular Vision|April 4, 2008
Autosomal dominant congenital cataract in a Libyan Jewish family: cosegregation with a reciprocal chromosomal translocation [t(3;5)(p22.3; p15.1)]Emre Zafer, Jeanne Meck, Liora Gerrad, et al.
Investigative Ophthalmology & Visual Science|May 27, 2004
A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataractsEran Pras, Judith Raz, Vered Yahalom, et al.
The American Journal of Cardiology|January 13, 2004
A novel form of familial bidirectional ventricular tachycardiaEyal Nof, Hadas Lahat, Naama Constantini, et al.
Autoimmunity Reviews|August 14, 2012
Incomplete response to colchicine in M694V homozygote FMF patientsMerav Lidar, Hagith Yonath, Naama Shechter, et al.
Molecular Vision|September 1, 2009
Cone-rod dystrophy and a frameshift mutation in the PROM1 geneEran Pras, Almogit Abu, Ygal Rotenstreich, et al.
Arthritis and Rheumatism|May 30, 2009
Clinical disease among patients heterozygous for familial Mediterranean feverDina Marek-Yagel, Yackov Berkun, Shai Padeh, et al.
Journal of Medical Genetics|May 20, 2015
Rare genetic variants in Tunisian Jewish patients suffering from age-related macular degenerationEran Pras, Dana Kristal, Nadav Shoshany, et al.
Pageof 11

Showing results (31-40 of 103) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|May 3, 2008
Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndromeAlmogit Abu, Moshe Frydman, Dina Marek, et al.
The Israel Medical Association Journal : IMAJ|June 26, 2017
Colorectal and Endometrial Cancer Risk and Age at Diagnosis in BLMAsh Mutation CarriersHagit Schayek, Yael Laitman, Lior H Katz, et al.
Seminars in Arthritis and Rheumatism|January 17, 2012
NOD2/CARD15 gene mutations in patients with familial Mediterranean feverYackov Berkun, Amir Karban, Shai Padeh, et al.
Molecular Vision|April 4, 2008
Autosomal dominant congenital cataract in a Libyan Jewish family: cosegregation with a reciprocal chromosomal translocation [t(3;5)(p22.3; p15.1)]Emre Zafer, Jeanne Meck, Liora Gerrad, et al.
Investigative Ophthalmology & Visual Science|May 27, 2004
A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataractsEran Pras, Judith Raz, Vered Yahalom, et al.
The American Journal of Cardiology|January 13, 2004
A novel form of familial bidirectional ventricular tachycardiaEyal Nof, Hadas Lahat, Naama Constantini, et al.
Autoimmunity Reviews|August 14, 2012
Incomplete response to colchicine in M694V homozygote FMF patientsMerav Lidar, Hagith Yonath, Naama Shechter, et al.
Molecular Vision|September 1, 2009
Cone-rod dystrophy and a frameshift mutation in the PROM1 geneEran Pras, Almogit Abu, Ygal Rotenstreich, et al.
Arthritis and Rheumatism|May 30, 2009
Clinical disease among patients heterozygous for familial Mediterranean feverDina Marek-Yagel, Yackov Berkun, Shai Padeh, et al.
Journal of Medical Genetics|May 20, 2015
Rare genetic variants in Tunisian Jewish patients suffering from age-related macular degenerationEran Pras, Dana Kristal, Nadav Shoshany, et al.
Pageof 11