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E Boltshauser

Showing results (71-80 of 214) with videos related to

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Archives of Disease in Childhood|January 1, 1988
Acrodermatitis chronica atrophicansD Nadal, R Gundelfinger, U Flueler, et al.
European Journal of Pediatrics|November 1, 1985
Craniosynostosis in hyper-IgE-syndromeP H Höger, E Boltshauser, W H Hitzig
Neuropediatrics|August 1, 1981
Sensory ganglioneuropathy in infantile spinal muscular atrophy. Light and electronmicroscopic findings in two casesA Probst, J Ulrich, A Bischoff, et al.
Schweizerische Medizinische Wochenschrift|May 25, 1996
[Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy]R Spiegel, A Hagmann, E Boltshauser, et al.
Schweizerische Medizinische Wochenschrift|January 9, 1988
[Childbirth in 2 patients with congenital analgesia]R Zimmermann, J Benz, J Gysel, et al.
Journal of Medical Genetics|February 1, 1989
Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy?E Boltshauser, W Lang, T Spillmann, et al.
Neurofibromatosis|January 1, 1989
Intracranial abnormalities associated with facial plexiform neurofibromas in neurofibromatosis type 1E Boltshauser, H Stocker, H Sailer, et al.
Schweizerische Medizinische Wochenschrift|December 17, 1977
[Kearns syndrome. Progressive external ophthalmoplegia, retinal pigment degeneration and heart conduction disorders]E Boltshauser, F Jerusalem, G Niemeyer, et al.
Neuropediatrics|February 1, 1996
Unilateral cerebellar aplasiaE Boltshauser, M Steinlin, E Martin, et al.
Human Molecular Genetics|September 1, 1993
Two novel mutations: 5108delAG and 5816insG in the NF1 gene detected by SSCP analysisJ Zhong, R Spiegel, E Boltshauser, et al.
Pageof 22

Showing results (71-80 of 214) with videos related to

Sort By:
Pageof 22
Archives of Disease in Childhood|January 1, 1988
Acrodermatitis chronica atrophicansD Nadal, R Gundelfinger, U Flueler, et al.
European Journal of Pediatrics|November 1, 1985
Craniosynostosis in hyper-IgE-syndromeP H Höger, E Boltshauser, W H Hitzig
Neuropediatrics|August 1, 1981
Sensory ganglioneuropathy in infantile spinal muscular atrophy. Light and electronmicroscopic findings in two casesA Probst, J Ulrich, A Bischoff, et al.
Schweizerische Medizinische Wochenschrift|May 25, 1996
[Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy]R Spiegel, A Hagmann, E Boltshauser, et al.
Schweizerische Medizinische Wochenschrift|January 9, 1988
[Childbirth in 2 patients with congenital analgesia]R Zimmermann, J Benz, J Gysel, et al.
Journal of Medical Genetics|February 1, 1989
Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy?E Boltshauser, W Lang, T Spillmann, et al.
Neurofibromatosis|January 1, 1989
Intracranial abnormalities associated with facial plexiform neurofibromas in neurofibromatosis type 1E Boltshauser, H Stocker, H Sailer, et al.
Schweizerische Medizinische Wochenschrift|December 17, 1977
[Kearns syndrome. Progressive external ophthalmoplegia, retinal pigment degeneration and heart conduction disorders]E Boltshauser, F Jerusalem, G Niemeyer, et al.
Neuropediatrics|February 1, 1996
Unilateral cerebellar aplasiaE Boltshauser, M Steinlin, E Martin, et al.
Human Molecular Genetics|September 1, 1993
Two novel mutations: 5108delAG and 5816insG in the NF1 gene detected by SSCP analysisJ Zhong, R Spiegel, E Boltshauser, et al.
Pageof 22