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

M Baraitser

Showing results (81-90 of 194) with videos related to

Pageof 20
Sort By:
Journal of Medical Genetics|April 1, 1984
A computerised data base for the diagnosis of rare dysmorphic syndromesR M Winter, M Baraitser, J M Douglas
Clinical Genetics|February 1, 1986
A family with congenital suprabulbar paresis (Worster-Drought syndrome)M A Patton, M Baraitser, E M Brett
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1989
A database of genetically determined neurological conditions for cliniciansM Baraitser, K Tomiwa, J Wilson, et al.
Journal of Medical Genetics|March 1, 1988
A reappraisal of the CHARGE associationC A Oley, M Baraitser, D B Grant
Clinical Dysmorphology|October 1, 1993
Kivlin syndrome and Peters'-Plus syndrome: are they the same disorder?E M Thompson, R M Winter, M Baraitser
Clinical Dysmorphology|October 1, 1993
Craniofrontonasal dysplasia in two male sibsU Natarajan, M Baraitser, K Nicolaides, et al.
British Medical Journal (Clinical Research Ed.)|January 22, 1983
Effect of genetic counselling on the prevalence of Huntington's choreaC O Carter, K A Evans, M Baraitser
Clinical Dysmorphology|January 1, 1996
Two brothers with deafness, femoral epiphyseal dysplasia, short stature and developmental delayL S Chitty, C M Hall, M Baraitser
Clinical Genetics|October 1, 1983
Greig cephalopolysyndactyly: report of 13 affected individuals in three familiesM Baraitser, R M Winter, E M Brett
Journal of Medical Genetics|June 1, 1983
Microcephaly and intracranial calcification in two brothersM Baraitser, E M Brett, A T Piesowicz
Pageof 20

Showing results (81-90 of 194) with videos related to

Sort By:
Pageof 20
Journal of Medical Genetics|April 1, 1984
A computerised data base for the diagnosis of rare dysmorphic syndromesR M Winter, M Baraitser, J M Douglas
Clinical Genetics|February 1, 1986
A family with congenital suprabulbar paresis (Worster-Drought syndrome)M A Patton, M Baraitser, E M Brett
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1989
A database of genetically determined neurological conditions for cliniciansM Baraitser, K Tomiwa, J Wilson, et al.
Journal of Medical Genetics|March 1, 1988
A reappraisal of the CHARGE associationC A Oley, M Baraitser, D B Grant
Clinical Dysmorphology|October 1, 1993
Kivlin syndrome and Peters'-Plus syndrome: are they the same disorder?E M Thompson, R M Winter, M Baraitser
Clinical Dysmorphology|October 1, 1993
Craniofrontonasal dysplasia in two male sibsU Natarajan, M Baraitser, K Nicolaides, et al.
British Medical Journal (Clinical Research Ed.)|January 22, 1983
Effect of genetic counselling on the prevalence of Huntington's choreaC O Carter, K A Evans, M Baraitser
Clinical Dysmorphology|January 1, 1996
Two brothers with deafness, femoral epiphyseal dysplasia, short stature and developmental delayL S Chitty, C M Hall, M Baraitser
Clinical Genetics|October 1, 1983
Greig cephalopolysyndactyly: report of 13 affected individuals in three familiesM Baraitser, R M Winter, E M Brett
Journal of Medical Genetics|June 1, 1983
Microcephaly and intracranial calcification in two brothersM Baraitser, E M Brett, A T Piesowicz
Pageof 20