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D A Marchuk

Showing results (11-20 of 70) with videos related to

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American Journal of Medical Genetics|March 21, 1998
Report on the workshop on Hereditary Hemorrhagic Telangiectasia, July 10-11, 1997D A Marchuk, A E Guttmacher, J A Penner, et al.
Nature Genetics|February 1, 1993
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesisE Legius, D A Marchuk, F S Collins, et al.
Human Molecular Genetics|November 5, 1999
Expression analysis of four endoglin missense mutations suggests that haploinsufficiency is the predominant mechanism for hereditary hemorrhagic telangiectasia type 1N Pece-Barbara, U Cymerman, S Vera, et al.
Journal of Medical Genetics|March 1, 1996
Clinical heterogeneity in hereditary haemorrhagic telangiectasia: are pulmonary arteriovenous malformations more common in families linked to endoglin?J N Berg, A E Guttmacher, D A Marchuk, et al.
Anticancer Research|November 1, 1995
Somatic mutations in the neurofibromatosis 1 gene in gliomas and primitive neuroectodermal tumoursG Thiel, K Marczinek, R Neumann, et al.
American Journal of Human Genetics|November 13, 2001
A second leaky splice-site mutation in the spastin geneI K Svenson, A E Ashley-Koch, M A Pericak-Vance, et al.
Human Molecular Genetics|July 1, 1993
A compound nucleotide repeat in the neurofibromatosis (NF1) geneL B Andersen, S A Tarlé, D A Marchuk, et al.
Human Molecular Genetics|May 1, 1993
Dinucleotide repeat polymorphism at the human erythropoietin receptor locus (EPOR) at 19p13M T McDonald, K A Papenberg, A A Glatfelter, et al.
American Journal of Medical Genetics|January 23, 1999
Genetic mapping of a novel familial form of infantile hemangiomaJ W Walter, F Blei, J L Anderson, et al.
American Journal of Medical Genetics|August 18, 2000
Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindredJ E McDonald, F J Miller, S E Hallam, et al.
Pageof 7

Showing results (11-20 of 70) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics|March 21, 1998
Report on the workshop on Hereditary Hemorrhagic Telangiectasia, July 10-11, 1997D A Marchuk, A E Guttmacher, J A Penner, et al.
Nature Genetics|February 1, 1993
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesisE Legius, D A Marchuk, F S Collins, et al.
Human Molecular Genetics|November 5, 1999
Expression analysis of four endoglin missense mutations suggests that haploinsufficiency is the predominant mechanism for hereditary hemorrhagic telangiectasia type 1N Pece-Barbara, U Cymerman, S Vera, et al.
Journal of Medical Genetics|March 1, 1996
Clinical heterogeneity in hereditary haemorrhagic telangiectasia: are pulmonary arteriovenous malformations more common in families linked to endoglin?J N Berg, A E Guttmacher, D A Marchuk, et al.
Anticancer Research|November 1, 1995
Somatic mutations in the neurofibromatosis 1 gene in gliomas and primitive neuroectodermal tumoursG Thiel, K Marczinek, R Neumann, et al.
American Journal of Human Genetics|November 13, 2001
A second leaky splice-site mutation in the spastin geneI K Svenson, A E Ashley-Koch, M A Pericak-Vance, et al.
Human Molecular Genetics|July 1, 1993
A compound nucleotide repeat in the neurofibromatosis (NF1) geneL B Andersen, S A Tarlé, D A Marchuk, et al.
Human Molecular Genetics|May 1, 1993
Dinucleotide repeat polymorphism at the human erythropoietin receptor locus (EPOR) at 19p13M T McDonald, K A Papenberg, A A Glatfelter, et al.
American Journal of Medical Genetics|January 23, 1999
Genetic mapping of a novel familial form of infantile hemangiomaJ W Walter, F Blei, J L Anderson, et al.
American Journal of Medical Genetics|August 18, 2000
Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindredJ E McDonald, F J Miller, S E Hallam, et al.
Pageof 7