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

Human genetics

Showing results (701-710 of 11,264) with videos related to

Pageof 1,127
Sort By:
Human Genetics|May 1, 1988
Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11M Andersson, D C Page, D Pettay, et al.
Human Genetics|April 9, 2020
The place of metropolitan France in the European genomic landscapeSimone Andrea Biagini, Eva Ramos-Luis, David Comas, et al.
Human Genetics|September 18, 2021
Classification of NF1 microdeletions and its importance for establishing genotype/phenotype correlations in patients with NF1 microdeletionsHildegard Kehrer-Sawatzki, David N Cooper
Human Genetics|September 18, 2021
Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in JapanYoh-Ichiro Iwasa, Shin-Ya Nishio, Hidekane Yoshimura, et al.
Human Genetics|September 13, 2021
Racial and ethnic disparities in diagnostic efficacy of comprehensive genetic testing for sensorineural hearing lossMichelle M Florentine, Stephanie L Rouse, Jihyun Stephans, et al.
Human Genetics|September 14, 2021
Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluationJohn Hoon Rim, Byunghwa Noh, Young Ik Koh, et al.
Human Genetics|January 1, 1984
The mode of inheritance of psoriasis: evidence for a major gene as well as a multifactorial component and its implication for genetic counsellingL Iselius, W R Williams
Human Genetics|January 1, 1984
Pure monosomy and trisomy 2q24.2----q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generationsM Moller, D García-Cruz, H Rivera, et al.
Human Genetics|January 1, 1984
Folic acid and chromosome breakage. II. A methionine effect similar to that in fragile X expressionJ A Reidy, A T Chen
Human Genetics|January 1, 1984
Human genes for glutathione S-transferasesV Laisney, Nguyen Van Cong, M S Gross, et al.
Pageof 1,127

Showing results (701-710 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|May 1, 1988
Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11M Andersson, D C Page, D Pettay, et al.
Human Genetics|April 9, 2020
The place of metropolitan France in the European genomic landscapeSimone Andrea Biagini, Eva Ramos-Luis, David Comas, et al.
Human Genetics|September 18, 2021
Classification of NF1 microdeletions and its importance for establishing genotype/phenotype correlations in patients with NF1 microdeletionsHildegard Kehrer-Sawatzki, David N Cooper
Human Genetics|September 18, 2021
Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in JapanYoh-Ichiro Iwasa, Shin-Ya Nishio, Hidekane Yoshimura, et al.
Human Genetics|September 13, 2021
Racial and ethnic disparities in diagnostic efficacy of comprehensive genetic testing for sensorineural hearing lossMichelle M Florentine, Stephanie L Rouse, Jihyun Stephans, et al.
Human Genetics|September 14, 2021
Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluationJohn Hoon Rim, Byunghwa Noh, Young Ik Koh, et al.
Human Genetics|January 1, 1984
The mode of inheritance of psoriasis: evidence for a major gene as well as a multifactorial component and its implication for genetic counsellingL Iselius, W R Williams
Human Genetics|January 1, 1984
Pure monosomy and trisomy 2q24.2----q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generationsM Moller, D García-Cruz, H Rivera, et al.
Human Genetics|January 1, 1984
Folic acid and chromosome breakage. II. A methionine effect similar to that in fragile X expressionJ A Reidy, A T Chen
Human Genetics|January 1, 1984
Human genes for glutathione S-transferasesV Laisney, Nguyen Van Cong, M S Gross, et al.
Pageof 1,127