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

C J de Weerdt

Showing results (1-10 of 20) with videos related to

Pageof 2
Sort By:
Journal of Medical Genetics|October 1, 1976
Linkage relations of locus for X-borne type of Charcot-Marie-Tooth muscular atrophy and that for Xg blood groupsC J de Weerdt
European Neurology|January 1, 1978
Charcot-Marie-Tooth disease with sex-linked inheritance, linkage studies and abnormal serum alkaline phosphatase levelsC J de Weerdt
Psychiatria, Neurologia, Neurochirurgia|March 1, 1972
A family with a progressive rigid-athetotic syndrome and dementiaC J de Weerdt
Nederlands Tijdschrift Voor Geneeskunde|September 9, 2000
[Epidermolysis bullosa simplex with progressive muscular dystrophy due to plectin deficiency]J Schuur, C J De Weerdt
Nederlands Tijdschrift Voor Geneeskunde|March 9, 1974
[Neurotoxic properties of dapsone]S Castelein, C J de Weerdt
Psychiatria, Neurologia, Neurochirurgia|July 1, 1972
Some aspects of heredity of brain tumoursC J de Weerdt, T Schut
European Neurology|January 1, 1974
Family with Charcot-Marie-Tooth disease showing unusual biochemical-clinical and genetic featuresC J de Weerdt, W Heerspink
Nederlands Tijdschrift Voor Geneeskunde|July 22, 1972
[Incidence of hereditary dystrophic bullous epidermolysis and progressive muscular dystrophy in one family]C J de Weerdt, S Castelein
Acta Neurologica Scandinavica|January 1, 1971
Neurological studies in families with Leber's optic atrophyC J de Weerdt, L N Went
Clinical Neurology and Neurosurgery|January 1, 1976
Congenital retarded myelinization in a new-born child with infantile spasmsC J de Weerdt, G J Hooghwinkel
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Journal of Medical Genetics|October 1, 1976
Linkage relations of locus for X-borne type of Charcot-Marie-Tooth muscular atrophy and that for Xg blood groupsC J de Weerdt
European Neurology|January 1, 1978
Charcot-Marie-Tooth disease with sex-linked inheritance, linkage studies and abnormal serum alkaline phosphatase levelsC J de Weerdt
Psychiatria, Neurologia, Neurochirurgia|March 1, 1972
A family with a progressive rigid-athetotic syndrome and dementiaC J de Weerdt
Nederlands Tijdschrift Voor Geneeskunde|September 9, 2000
[Epidermolysis bullosa simplex with progressive muscular dystrophy due to plectin deficiency]J Schuur, C J De Weerdt
Nederlands Tijdschrift Voor Geneeskunde|March 9, 1974
[Neurotoxic properties of dapsone]S Castelein, C J de Weerdt
Psychiatria, Neurologia, Neurochirurgia|July 1, 1972
Some aspects of heredity of brain tumoursC J de Weerdt, T Schut
European Neurology|January 1, 1974
Family with Charcot-Marie-Tooth disease showing unusual biochemical-clinical and genetic featuresC J de Weerdt, W Heerspink
Nederlands Tijdschrift Voor Geneeskunde|July 22, 1972
[Incidence of hereditary dystrophic bullous epidermolysis and progressive muscular dystrophy in one family]C J de Weerdt, S Castelein
Acta Neurologica Scandinavica|January 1, 1971
Neurological studies in families with Leber's optic atrophyC J de Weerdt, L N Went
Clinical Neurology and Neurosurgery|January 1, 1976
Congenital retarded myelinization in a new-born child with infantile spasmsC J de Weerdt, G J Hooghwinkel
Pageof 2