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

Clinical genetics

Showing results (441-450 of 7,173) with videos related to

Pageof 718
Sort By:
Clinical Genetics|March 1, 1987
Roberts syndrome and SC phocomelia. A single genetic entityC Römke, U Froster-Iskenius, K Heyne, et al.
Clinical Genetics|March 1, 1987
Cerebellar ataxia and total albinismR Bamezai, S A Husain, S Misra, et al.
Clinical Genetics|March 1, 1987
Major genes of eye color and hair color linked to LU and SEH Eiberg, J Mohr
Clinical Genetics|June 27, 2022
The first Chinese case of Siddiqi syndrome caused by a homozygous FITM2 variantYunting Lin, Wen Zhang, Duan Li, et al.
Clinical Genetics|November 29, 2022
Novel de novo ZNF148 truncating variant causing autism spectrum disorder, attention deficit hyperactivity disorder, and intellectual disabilityChunyue Miao, Lin Du, Yu Zhang, et al.
Clinical Genetics|August 1, 1987
Incidence of familial dysautonomia in Israel 1977-1981C Maayan, E Kaplan, S Shachar, et al.
Clinical Genetics|August 1, 1987
Effect of combinations of antioxidants on oxygen radical-induced sister chromatid exchangesA B Weitberg
Clinical Genetics|August 1, 1987
X-linked myotubular myopathy: intrafamilial variability and normal muscle biopsy in a heterozygous femaleL D Keppen, M M Husain, R C Woody
Clinical Genetics|December 17, 2022
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotypeJiaxin He, Qiang Liu, Weili Wang, et al.
Clinical Genetics|January 3, 2023
Novel variants in ACTL7A and PLCZ1 are associated with male infertility and total fertilization failureShuai Zhao, Ying Cui, Shunli Guo, et al.
Pageof 718

Showing results (441-450 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|March 1, 1987
Roberts syndrome and SC phocomelia. A single genetic entityC Römke, U Froster-Iskenius, K Heyne, et al.
Clinical Genetics|March 1, 1987
Cerebellar ataxia and total albinismR Bamezai, S A Husain, S Misra, et al.
Clinical Genetics|March 1, 1987
Major genes of eye color and hair color linked to LU and SEH Eiberg, J Mohr
Clinical Genetics|June 27, 2022
The first Chinese case of Siddiqi syndrome caused by a homozygous FITM2 variantYunting Lin, Wen Zhang, Duan Li, et al.
Clinical Genetics|November 29, 2022
Novel de novo ZNF148 truncating variant causing autism spectrum disorder, attention deficit hyperactivity disorder, and intellectual disabilityChunyue Miao, Lin Du, Yu Zhang, et al.
Clinical Genetics|August 1, 1987
Incidence of familial dysautonomia in Israel 1977-1981C Maayan, E Kaplan, S Shachar, et al.
Clinical Genetics|August 1, 1987
Effect of combinations of antioxidants on oxygen radical-induced sister chromatid exchangesA B Weitberg
Clinical Genetics|August 1, 1987
X-linked myotubular myopathy: intrafamilial variability and normal muscle biopsy in a heterozygous femaleL D Keppen, M M Husain, R C Woody
Clinical Genetics|December 17, 2022
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotypeJiaxin He, Qiang Liu, Weili Wang, et al.
Clinical Genetics|January 3, 2023
Novel variants in ACTL7A and PLCZ1 are associated with male infertility and total fertilization failureShuai Zhao, Ying Cui, Shunli Guo, et al.
Pageof 718