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

Lavinia Caba

Showing results (31-40 of 34) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 34 results.
Genes|December 18, 2020
Genetics of Hearing Impairment in North-Eastern Romania-A Cost-Effective Improved Diagnosis and Literature ReviewIrina Resmerita, Romica Sebastian Cozma, Roxana Popescu, et al.
Diagnostics (Basel, Switzerland)|September 28, 2021
Novel Mutation in <i>APC</i> Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner SyndromeCristina Antohi, Danisia Haba, Lavinia Caba, et al.
Genes|December 24, 2021
A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the LiteratureRoxana Popescu, Mihaela Grămescu, Lavinia Caba, et al.
American Journal of Medical Genetics. Part A|June 9, 2023
Exome sequencing in a Romanian Bardet-Biedl syndrome cohort revealed an overabundance of causal BBS12 variantsSheraz Khan, Ina Ofelia Focșa, Magdalena Budișteanu, et al.
Pageof 4

Showing results (31-40 of 34) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 34 results.
Genes|December 18, 2020
Genetics of Hearing Impairment in North-Eastern Romania-A Cost-Effective Improved Diagnosis and Literature ReviewIrina Resmerita, Romica Sebastian Cozma, Roxana Popescu, et al.
Diagnostics (Basel, Switzerland)|September 28, 2021
Novel Mutation in <i>APC</i> Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner SyndromeCristina Antohi, Danisia Haba, Lavinia Caba, et al.
Genes|December 24, 2021
A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the LiteratureRoxana Popescu, Mihaela Grămescu, Lavinia Caba, et al.
American Journal of Medical Genetics. Part A|June 9, 2023
Exome sequencing in a Romanian Bardet-Biedl syndrome cohort revealed an overabundance of causal BBS12 variantsSheraz Khan, Ina Ofelia Focșa, Magdalena Budișteanu, et al.
Pageof 4