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C Verellen

Showing results (41-50 of 77) with videos related to

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Muscle & Nerve|September 1, 1979
Serum creatine kinase and pyruvate kinase in Duchenne muscular dystrophy carrier detectionM E Percy, L S Chang, E G Murphy, et al.
Human Genetics|October 28, 1997
Novel germline mutations in the APC gene and their phenotypic spectrum in familial adenomatous polyposis kindredsC Walon, A Kartheuser, G Michils, et al.
Lancet (London, England)|March 12, 1999
New possibilities for prenatal diagnosis of muscular dystrophies: forced myogenesis with an adenoviral MyoD-vectorP A Roest, E Bakker, F J Fallaux, et al.
Journal of Medical Genetics|December 1, 1986
Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophyV M Kean, H L Macleod, M W Thompson, et al.
B-ENT|March 21, 2007
Orofacial clefting: update on the role of geneticsM Ghassibe, B Bayet, N Revencu, et al.
Pediatric Hematology and Oncology|July 1, 1991
Leiomyoma of the suprarenal gland in a child with ataxia-telangiectasiaF Mouchet, J Ninane, S Gosseye, et al.
International Journal of Nuclear Medicine and Biology|January 1, 1981
Gallium-67 citrate localization in carriers of Duchenne muscular dystrophyR G Brown, J M Ash, C Verellen-Dumoulin, et al.
Cancer Genetics and Cytogenetics|July 21, 2001
Trisomy 16 as the sole anomaly in hematological malignancies. Three new cases and a short reviewB Guillaume, G Ameye, J Dierlamm, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
A D255H substitution in the arylsulphatase A gene of two unrelated Belgian patients with late-infantile metachromatic leukodystrophyW Lissens, R Vervoort, N Van Regemorter, et al.
Nature Genetics|June 1, 1992
Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxisB V Nusgens, C Verellen-Dumoulin, T Hermanns-Lê, et al.
Pageof 8

Showing results (41-50 of 77) with videos related to

Sort By:
Pageof 8
Muscle & Nerve|September 1, 1979
Serum creatine kinase and pyruvate kinase in Duchenne muscular dystrophy carrier detectionM E Percy, L S Chang, E G Murphy, et al.
Human Genetics|October 28, 1997
Novel germline mutations in the APC gene and their phenotypic spectrum in familial adenomatous polyposis kindredsC Walon, A Kartheuser, G Michils, et al.
Lancet (London, England)|March 12, 1999
New possibilities for prenatal diagnosis of muscular dystrophies: forced myogenesis with an adenoviral MyoD-vectorP A Roest, E Bakker, F J Fallaux, et al.
Journal of Medical Genetics|December 1, 1986
Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophyV M Kean, H L Macleod, M W Thompson, et al.
B-ENT|March 21, 2007
Orofacial clefting: update on the role of geneticsM Ghassibe, B Bayet, N Revencu, et al.
Pediatric Hematology and Oncology|July 1, 1991
Leiomyoma of the suprarenal gland in a child with ataxia-telangiectasiaF Mouchet, J Ninane, S Gosseye, et al.
International Journal of Nuclear Medicine and Biology|January 1, 1981
Gallium-67 citrate localization in carriers of Duchenne muscular dystrophyR G Brown, J M Ash, C Verellen-Dumoulin, et al.
Cancer Genetics and Cytogenetics|July 21, 2001
Trisomy 16 as the sole anomaly in hematological malignancies. Three new cases and a short reviewB Guillaume, G Ameye, J Dierlamm, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
A D255H substitution in the arylsulphatase A gene of two unrelated Belgian patients with late-infantile metachromatic leukodystrophyW Lissens, R Vervoort, N Van Regemorter, et al.
Nature Genetics|June 1, 1992
Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxisB V Nusgens, C Verellen-Dumoulin, T Hermanns-Lê, et al.
Pageof 8