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D A Marchuk

Showing results (21-30 of 70) with videos related to

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Human Genetics|December 1, 1993
An EcoRI RFLP in the 5' region of the human NF1 geneE Reyniers, K De Boulle, D A Marchuk, et al.
Acta Neurochirurgica. Supplement|December 11, 2008
Genetic considerations relevant to intracranial hemorrhage and brain arteriovenous malformationsH Kim, D A Marchuk, L Pawlikowska, et al.
Orphanet Journal of Rare Diseases|November 7, 2022
Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasiaK P Thompson, J Sykes, P Chandakkar, et al.
Orphanet Journal of Rare Diseases|January 7, 2021
Predictors of mortality in patients with hereditary hemorrhagic telangiectasiaK P Thompson, J Nelson, H Kim, et al.
Cancer Genetics and Cytogenetics|March 1, 1996
Chromosome breakpoint at 17q11.2 and insertion of DNA from three different chromosomes in a glioblastoma with exceptional glial fibrillary acidic protein expressionP E McKeever, T R Dennis, A C Burgess, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 2, 2003
Impact of genetic polymorphisms on heart failure prognosisP Le Corvoisier, H Y Park, K M Carlson, et al.
Journal of Medical Genetics|September 10, 2003
Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational classA G Yip, A Dürr, D A Marchuk, et al.
Nucleic Acids Research|July 11, 1991
A highly polymorphic cDNA probe in the NF1 geneL B Andersen, M R Wallace, D A Marchuk, et al.
Genomics|October 1, 1992
The gene for a novel epidermal antigen maps near the neurofibromatosis 1 geneL M Kayes, W T Schroeder, D A Marchuk, et al.
Human Genetics|September 12, 2000
Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles: evidence for a founder effectC J Gallione, E A Scheessele, D Reinhardt, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

Sort By:
Pageof 7
Human Genetics|December 1, 1993
An EcoRI RFLP in the 5' region of the human NF1 geneE Reyniers, K De Boulle, D A Marchuk, et al.
Acta Neurochirurgica. Supplement|December 11, 2008
Genetic considerations relevant to intracranial hemorrhage and brain arteriovenous malformationsH Kim, D A Marchuk, L Pawlikowska, et al.
Orphanet Journal of Rare Diseases|November 7, 2022
Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasiaK P Thompson, J Sykes, P Chandakkar, et al.
Orphanet Journal of Rare Diseases|January 7, 2021
Predictors of mortality in patients with hereditary hemorrhagic telangiectasiaK P Thompson, J Nelson, H Kim, et al.
Cancer Genetics and Cytogenetics|March 1, 1996
Chromosome breakpoint at 17q11.2 and insertion of DNA from three different chromosomes in a glioblastoma with exceptional glial fibrillary acidic protein expressionP E McKeever, T R Dennis, A C Burgess, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 2, 2003
Impact of genetic polymorphisms on heart failure prognosisP Le Corvoisier, H Y Park, K M Carlson, et al.
Journal of Medical Genetics|September 10, 2003
Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational classA G Yip, A Dürr, D A Marchuk, et al.
Nucleic Acids Research|July 11, 1991
A highly polymorphic cDNA probe in the NF1 geneL B Andersen, M R Wallace, D A Marchuk, et al.
Genomics|October 1, 1992
The gene for a novel epidermal antigen maps near the neurofibromatosis 1 geneL M Kayes, W T Schroeder, D A Marchuk, et al.
Human Genetics|September 12, 2000
Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles: evidence for a founder effectC J Gallione, E A Scheessele, D Reinhardt, et al.
Pageof 7