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 (591-600 of 7,173) with videos related to

Pageof 718
Sort By:
Clinical Genetics|July 25, 2000
Maternally inherited hearing impairmentG Van Camp, R J Smith
Clinical Genetics|February 1, 1975
Incontinentia pigmentiT Iancu, L Komlos, F Shabtay, et al.
Clinical Genetics|February 1, 1975
Genetics of acheiropodia (the handless and footless families of Brazil)A Freire-Maia
Clinical Genetics|March 1, 1975
The significance of "unspecific neuropathy" in hereditary ataxias and related disordersH Skre
Clinical Genetics|March 1, 1975
Familial occurrence of the g syndromeJ P van Biervliet, J O van Hemel
Clinical Genetics|March 29, 2000
Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotypeC Prasad, A N Prasad, B N Chodirker, et al.
Clinical Genetics|March 25, 2000
Caspases and neurodegeneration: on the cutting edge of new therapeutic approachesC L Wellington, M R Hayden
Clinical Genetics|March 25, 2000
Partial CFTR genotyping and characterisation of cystic fibrosis patients with myocardial fibrosis and necrosisJ Zebrak, B Skuza, A Pogorzelski, et al.
Clinical Genetics|March 25, 2000
An SRY-negative XX male with Huriez syndromeP Vernole, A Terrinoni, B Didona, et al.
Clinical Genetics|May 1, 1975
Serum esterases of Icelanders. I. A "silent" pseudocholinesterase gene in an Icelandic familyA Arnason, O Jensson, S Gudmundsson
Pageof 718

Showing results (591-600 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|July 25, 2000
Maternally inherited hearing impairmentG Van Camp, R J Smith
Clinical Genetics|February 1, 1975
Incontinentia pigmentiT Iancu, L Komlos, F Shabtay, et al.
Clinical Genetics|February 1, 1975
Genetics of acheiropodia (the handless and footless families of Brazil)A Freire-Maia
Clinical Genetics|March 1, 1975
The significance of "unspecific neuropathy" in hereditary ataxias and related disordersH Skre
Clinical Genetics|March 1, 1975
Familial occurrence of the g syndromeJ P van Biervliet, J O van Hemel
Clinical Genetics|March 29, 2000
Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotypeC Prasad, A N Prasad, B N Chodirker, et al.
Clinical Genetics|March 25, 2000
Caspases and neurodegeneration: on the cutting edge of new therapeutic approachesC L Wellington, M R Hayden
Clinical Genetics|March 25, 2000
Partial CFTR genotyping and characterisation of cystic fibrosis patients with myocardial fibrosis and necrosisJ Zebrak, B Skuza, A Pogorzelski, et al.
Clinical Genetics|March 25, 2000
An SRY-negative XX male with Huriez syndromeP Vernole, A Terrinoni, B Didona, et al.
Clinical Genetics|May 1, 1975
Serum esterases of Icelanders. I. A "silent" pseudocholinesterase gene in an Icelandic familyA Arnason, O Jensson, S Gudmundsson
Pageof 718