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 (341-350 of 7,173) with videos related to

Pageof 718
Sort By:
Clinical Genetics|March 13, 2021
Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in IranMarzieh Mohseni, Mojgan Babanejad, Kevin T Booth, et al.
Clinical Genetics|February 14, 2021
Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failureMaryam Rezaei, Beena Suresh, Eric Bereke, et al.
Clinical Genetics|February 1, 1988
EEC syndrome sine sine? Report of a family with oligosymptomatic EEC syndromeF Majewski, W Küster
Clinical Genetics|March 1, 1988
Discriminant analysis of dermatoglyphic measurements in fragile X males and femalesD Z Loesch
Clinical Genetics|March 1, 1988
Partial duplication of the eyebrows with other congenital malformations: a new syndromeM Berkenstadt, H Zahavie, R M Goodman
Clinical Genetics|March 1, 1988
Life-span and Menkes kinky hair syndrome: report of a 13-year course of this diseaseC Sander, H Niederhoff, N Horn
Clinical Genetics|February 23, 2021
De novo variants in neurodevelopmental disorders-experiences from a tertiary care centerTheresa Brunet, Robert Jech, Melanie Brugger, et al.
Clinical Genetics|May 1, 1987
Syndrome of microcephaly, deafness/malformed ears, mental retardation and peculiar facies in a mother and sonH Kawashima, N Tsuji
Clinical Genetics|May 1, 1987
Fragile sites are unrelated to reciprocal translocation breakpointsJ R Davis, R M Hagaman
Clinical Genetics|May 1, 1987
Trichodysplasia-xeroderma: an autosomal dominant conditionM Pinheiro, N Freire-Maia
Pageof 718

Showing results (341-350 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|March 13, 2021
Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in IranMarzieh Mohseni, Mojgan Babanejad, Kevin T Booth, et al.
Clinical Genetics|February 14, 2021
Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failureMaryam Rezaei, Beena Suresh, Eric Bereke, et al.
Clinical Genetics|February 1, 1988
EEC syndrome sine sine? Report of a family with oligosymptomatic EEC syndromeF Majewski, W Küster
Clinical Genetics|March 1, 1988
Discriminant analysis of dermatoglyphic measurements in fragile X males and femalesD Z Loesch
Clinical Genetics|March 1, 1988
Partial duplication of the eyebrows with other congenital malformations: a new syndromeM Berkenstadt, H Zahavie, R M Goodman
Clinical Genetics|March 1, 1988
Life-span and Menkes kinky hair syndrome: report of a 13-year course of this diseaseC Sander, H Niederhoff, N Horn
Clinical Genetics|February 23, 2021
De novo variants in neurodevelopmental disorders-experiences from a tertiary care centerTheresa Brunet, Robert Jech, Melanie Brugger, et al.
Clinical Genetics|May 1, 1987
Syndrome of microcephaly, deafness/malformed ears, mental retardation and peculiar facies in a mother and sonH Kawashima, N Tsuji
Clinical Genetics|May 1, 1987
Fragile sites are unrelated to reciprocal translocation breakpointsJ R Davis, R M Hagaman
Clinical Genetics|May 1, 1987
Trichodysplasia-xeroderma: an autosomal dominant conditionM Pinheiro, N Freire-Maia
Pageof 718