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H Zellweger

Showing results (61-70 of 117) with videos related to

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Journal of the Iowa Medical Society|September 1, 1971
Prenatal genetics and cytogeneticsH Zellweger, C White, R Kretzschmar
Lancet (London, England)|January 31, 1976
Letter: Parental consanguinity in pycnodysostosisM Waziri, H Zellweger, J Seibert
Helvetica Paediatrica Acta|September 1, 1980
Sporadic Duchenne muscular dystrophy in females; genetic counseling of women with pelvifemoral muscular dystrophyH Zellweger, V Ionasescu, J Simpson
Acta Neurologica Scandinavica|November 1, 1976
Detection of carriers and genetic counseling in duchenne muscular dystrophy by ribosomal protein synthesisV Ionasescu, H Zellweger, L Burmeister
American Journal of Diseases of Children (1960)|September 1, 1976
Teratogenic effect of anticonvulsant drugsM Waziri, V Ionasescu, H Zellweger
Acta Neurologica Scandinavica|January 1, 1972
The diagnostic significance of serum enzymes and electrocardiogram in various muscular dystrophiesH Zellweger, R Durnin, J Simpson
Journal of Medical Genetics|December 1, 1972
A new genetic variant of the spinal muscular atrophies in infancyH Zellweger, E Hanhart, H J Schneider
Neurology|July 1, 1971
A new approach for carrier detection in Duchenne muscular dystrophy. Protein synthesis of muscle polyribosomes in vitroV Ionasescu, H Zellweger, T W Conway
The Journal of Pediatrics|June 1, 1974
The Marshall syndrome: report of a new familyH Zellweger, J K Smith, P Grützner
Schweizerische Medizinische Wochenschrift|June 3, 1972
[Muscular dystrophies]H Zellweger, V Ionasescu, T W Conway
Pageof 12

Showing results (61-70 of 117) with videos related to

Sort By:
Pageof 12
Journal of the Iowa Medical Society|September 1, 1971
Prenatal genetics and cytogeneticsH Zellweger, C White, R Kretzschmar
Lancet (London, England)|January 31, 1976
Letter: Parental consanguinity in pycnodysostosisM Waziri, H Zellweger, J Seibert
Helvetica Paediatrica Acta|September 1, 1980
Sporadic Duchenne muscular dystrophy in females; genetic counseling of women with pelvifemoral muscular dystrophyH Zellweger, V Ionasescu, J Simpson
Acta Neurologica Scandinavica|November 1, 1976
Detection of carriers and genetic counseling in duchenne muscular dystrophy by ribosomal protein synthesisV Ionasescu, H Zellweger, L Burmeister
American Journal of Diseases of Children (1960)|September 1, 1976
Teratogenic effect of anticonvulsant drugsM Waziri, V Ionasescu, H Zellweger
Acta Neurologica Scandinavica|January 1, 1972
The diagnostic significance of serum enzymes and electrocardiogram in various muscular dystrophiesH Zellweger, R Durnin, J Simpson
Journal of Medical Genetics|December 1, 1972
A new genetic variant of the spinal muscular atrophies in infancyH Zellweger, E Hanhart, H J Schneider
Neurology|July 1, 1971
A new approach for carrier detection in Duchenne muscular dystrophy. Protein synthesis of muscle polyribosomes in vitroV Ionasescu, H Zellweger, T W Conway
The Journal of Pediatrics|June 1, 1974
The Marshall syndrome: report of a new familyH Zellweger, J K Smith, P Grützner
Schweizerische Medizinische Wochenschrift|June 3, 1972
[Muscular dystrophies]H Zellweger, V Ionasescu, T W Conway
Pageof 12