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C Hamel

Showing results (261-270 of 291) with videos related to

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Genomics|March 1, 1997
Cloning of the genes encoding two murine and human cochlear unconventional type I myosinsF Crozet, A el Amraoui, S Blanchard, et al.
Clinical Genetics|August 8, 2009
Neuromuscular features in Marfan syndromeN c Voermans, J Timmermans, N van Alfen, et al.
Phlebology|April 6, 2013
European guidelines for sclerotherapy in chronic venous disordersE Rabe, F X Breu, A Cavezzi, et al.
Journal of Medical Genetics|January 15, 2003
Recessive multiple epiphyseal dysplasia (rMED): phenotype delineation in eighteen homozygotes for DTDST mutation R279WD Ballhausen, L Bonafé, P Terhal, et al.
Bioorganic & Medicinal Chemistry Letters|November 19, 2003
The synthesis and antibacterial activity of 1,3,4-thiadiazole phenyl oxazolidinone analoguesLisa M Thomasco, Robert C Gadwood, Elizabeth A Weaver, et al.
American Journal of Medical Genetics|July 31, 2001
Meier-Gorlin syndrome: report of eight additional cases and reviewE M Bongers, J M Opitz, A Fryer, et al.
Gene Therapy|October 7, 2006
Restoration of vision in RPE65-deficient Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epitheliumG Le Meur, K Stieger, A J Smith, et al.
American Journal of Medical Genetics|July 9, 1999
Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysisB C Hamel, A P Smits, B van den Helm, et al.
Systematic Reviews|August 5, 2024
Comparative effectiveness of interventions for cancer treatment-related cognitive impairment in adult cancer survivors: protocol for a systematic reviewD M Wolfe, C Hamel, D Rice, et al.
Nature Genetics|October 4, 2000
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardationK Kutsche, H Yntema, A Brandt, et al.
Pageof 30

Showing results (261-270 of 291) with videos related to

Sort By:
Pageof 30
Genomics|March 1, 1997
Cloning of the genes encoding two murine and human cochlear unconventional type I myosinsF Crozet, A el Amraoui, S Blanchard, et al.
Clinical Genetics|August 8, 2009
Neuromuscular features in Marfan syndromeN c Voermans, J Timmermans, N van Alfen, et al.
Phlebology|April 6, 2013
European guidelines for sclerotherapy in chronic venous disordersE Rabe, F X Breu, A Cavezzi, et al.
Journal of Medical Genetics|January 15, 2003
Recessive multiple epiphyseal dysplasia (rMED): phenotype delineation in eighteen homozygotes for DTDST mutation R279WD Ballhausen, L Bonafé, P Terhal, et al.
Bioorganic & Medicinal Chemistry Letters|November 19, 2003
The synthesis and antibacterial activity of 1,3,4-thiadiazole phenyl oxazolidinone analoguesLisa M Thomasco, Robert C Gadwood, Elizabeth A Weaver, et al.
American Journal of Medical Genetics|July 31, 2001
Meier-Gorlin syndrome: report of eight additional cases and reviewE M Bongers, J M Opitz, A Fryer, et al.
Gene Therapy|October 7, 2006
Restoration of vision in RPE65-deficient Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epitheliumG Le Meur, K Stieger, A J Smith, et al.
American Journal of Medical Genetics|July 9, 1999
Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysisB C Hamel, A P Smits, B van den Helm, et al.
Systematic Reviews|August 5, 2024
Comparative effectiveness of interventions for cancer treatment-related cognitive impairment in adult cancer survivors: protocol for a systematic reviewD M Wolfe, C Hamel, D Rice, et al.
Nature Genetics|October 4, 2000
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardationK Kutsche, H Yntema, A Brandt, et al.
Pageof 30