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American Journal of Human Genetics|July 1, 1997

The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2J N Berg, C J Gallione, T T Stenzel, et al.

Journal of Medical Genetics|March 1, 1995

A gene for familial venous malformations maps to chromosome 9p in a second large kindredC J Gallione, K A Pasyk, L M Boon, et al.

Nature Genetics|December 1, 1994

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1K A McAllister, K M Grogg, D W Johnson, et al.

Human Genetics|April 1, 1998

Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant diseaseK F Damji, C J Gallione, R R Allingham, et al.

Genome Research|August 1, 1995

A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12D W Johnson, J N Berg, C J Gallione, et al.

Genomics|July 20, 1995

A locus for cerebral cavernous malformations maps to chromosome 7q in two familiesD A Marchuk, C J Gallione, L A Morrison, et al.

Journal of Medical Genetics|April 15, 2006

SMAD4 mutations found in unselected HHT patientsC J Gallione, J A Richards, T G W Letteboer, et al.

Nature Genetics|June 1, 1996

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2D W Johnson, J N Berg, M A Baldwin, et al.

Human Mutation|April 29, 1998

Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null allelesC J Gallione, D J Klaus, E Y Yeh, et al.

Human Molecular Genetics|November 5, 1999

Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)T Sahoo, E W Johnson, J W Thomas, et al.

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

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 20 results.

American Journal of Human Genetics|July 1, 1997

The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2J N Berg, C J Gallione, T T Stenzel, et al.

Journal of Medical Genetics|March 1, 1995

A gene for familial venous malformations maps to chromosome 9p in a second large kindredC J Gallione, K A Pasyk, L M Boon, et al.

Nature Genetics|December 1, 1994

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1K A McAllister, K M Grogg, D W Johnson, et al.

Human Genetics|April 1, 1998

Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant diseaseK F Damji, C J Gallione, R R Allingham, et al.

Genome Research|August 1, 1995

A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12D W Johnson, J N Berg, C J Gallione, et al.

Genomics|July 20, 1995

A locus for cerebral cavernous malformations maps to chromosome 7q in two familiesD A Marchuk, C J Gallione, L A Morrison, et al.

Journal of Medical Genetics|April 15, 2006

SMAD4 mutations found in unselected HHT patientsC J Gallione, J A Richards, T G W Letteboer, et al.

Nature Genetics|June 1, 1996

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2D W Johnson, J N Berg, M A Baldwin, et al.

Human Mutation|April 29, 1998

Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null allelesC J Gallione, D J Klaus, E Y Yeh, et al.

Human Molecular Genetics|November 5, 1999

Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)T Sahoo, E W Johnson, J W Thomas, et al.

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