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 (111-120 of 194) with videos related to

Pageof 20
Sort By:
Neuropediatrics|November 1, 1987
The use of a computerised database for the diagnosis of a rare neurological syndromeK Tomiwa, M Baraitser, E M Brett, et al.
Clinical Genetics|August 1, 1986
A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infectionJ Burn, H T Wickramasinghe, B Harding, et al.
Journal of Medical Genetics|June 1, 1984
Orofaciodigital syndrome with mesomelic limb shorteningJ Burn, C Dezateux, C M Hall, et al.
Clinical Genetics|March 1, 1991
Atypical facio-scapulo-humeral muscular dystrophy--a counselling dilemmaW Reardon, I K Temple, G Harwood, et al.
Journal of Medical Genetics|September 1, 1991
Sibs with mental retardation, supraorbital sclerosis, and metaphyseal dysplasia: frontometaphyseal dysplasia, craniometaphyseal dysplasia, or a new syndrome?W Reardon, C M Hall, M J Dillon, et al.
Journal of Medical Genetics|March 1, 1992
Distal spinal muscular atrophy with vocal cord paralysisC Pridmore, M Baraitser, E M Brett, et al.
Journal of Medical Genetics|April 1, 1985
The clinical features of the Cohen syndrome: further case reportsC North, M A Patton, M Baraitser, et al.
Archives of Disease in Childhood|September 1, 1990
The iris in Williams syndromeG Holmström, G Almond, K Temple, et al.
Clinical Dysmorphology|April 1, 1993
Congenital cataract, microphthalmia and septal heart defect in two generations: a new syndrome?A O Wilkie, D Taylor, P J Scambler, et al.
Journal of Medical Genetics|June 1, 1990
Proteus syndrome: report of a case with severe brain impairment and fatal courseR Rizzo, L Pavone, G Sorge, et al.
Pageof 20

Showing results (111-120 of 194) with videos related to

Sort By:
Pageof 20
Neuropediatrics|November 1, 1987
The use of a computerised database for the diagnosis of a rare neurological syndromeK Tomiwa, M Baraitser, E M Brett, et al.
Clinical Genetics|August 1, 1986
A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infectionJ Burn, H T Wickramasinghe, B Harding, et al.
Journal of Medical Genetics|June 1, 1984
Orofaciodigital syndrome with mesomelic limb shorteningJ Burn, C Dezateux, C M Hall, et al.
Clinical Genetics|March 1, 1991
Atypical facio-scapulo-humeral muscular dystrophy--a counselling dilemmaW Reardon, I K Temple, G Harwood, et al.
Journal of Medical Genetics|September 1, 1991
Sibs with mental retardation, supraorbital sclerosis, and metaphyseal dysplasia: frontometaphyseal dysplasia, craniometaphyseal dysplasia, or a new syndrome?W Reardon, C M Hall, M J Dillon, et al.
Journal of Medical Genetics|March 1, 1992
Distal spinal muscular atrophy with vocal cord paralysisC Pridmore, M Baraitser, E M Brett, et al.
Journal of Medical Genetics|April 1, 1985
The clinical features of the Cohen syndrome: further case reportsC North, M A Patton, M Baraitser, et al.
Archives of Disease in Childhood|September 1, 1990
The iris in Williams syndromeG Holmström, G Almond, K Temple, et al.
Clinical Dysmorphology|April 1, 1993
Congenital cataract, microphthalmia and septal heart defect in two generations: a new syndrome?A O Wilkie, D Taylor, P J Scambler, et al.
Journal of Medical Genetics|June 1, 1990
Proteus syndrome: report of a case with severe brain impairment and fatal courseR Rizzo, L Pavone, G Sorge, et al.
Pageof 20