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D A Marchuk

Showing results (51-60 of 70) with videos related to

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Science (New York, N.Y.)|July 13, 1990
Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patientsM R Wallace, D A Marchuk, L B Andersen, et al.
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.
Genomics|July 1, 1992
A yeast artificial chromosome contig encompassing the type 1 neurofibromatosis geneD A Marchuk, R Tavakkol, M R Wallace, 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.
Journal of Medical Genetics|December 1, 1994
Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotypeK A McAllister, F Lennon, B Bowles-Biesecker, et al.
Developmental Biology|January 8, 2000
Endoglin, an ancillary TGFbeta receptor, is required for extraembryonic angiogenesis and plays a key role in heart developmentH M Arthur, J Ure, A J Smith, et al.
Human Heredity|February 15, 2001
Additional glomangioma families link to chromosome 1p: no evidence for genetic heterogeneityJ T Calvert, S Burns, T J Riney, 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.
Genomics|February 13, 2001
Computational and experimental analyses reveal previously undetected coding exons of the KRIT1 (CCM1) geneT Sahoo, E Goenaga-Diaz, I G Serebriiskii, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Science (New York, N.Y.)|July 13, 1990
Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patientsM R Wallace, D A Marchuk, L B Andersen, et al.
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.
Genomics|July 1, 1992
A yeast artificial chromosome contig encompassing the type 1 neurofibromatosis geneD A Marchuk, R Tavakkol, M R Wallace, 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.
Journal of Medical Genetics|December 1, 1994
Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotypeK A McAllister, F Lennon, B Bowles-Biesecker, et al.
Developmental Biology|January 8, 2000
Endoglin, an ancillary TGFbeta receptor, is required for extraembryonic angiogenesis and plays a key role in heart developmentH M Arthur, J Ure, A J Smith, et al.
Human Heredity|February 15, 2001
Additional glomangioma families link to chromosome 1p: no evidence for genetic heterogeneityJ T Calvert, S Burns, T J Riney, 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.
Genomics|February 13, 2001
Computational and experimental analyses reveal previously undetected coding exons of the KRIT1 (CCM1) geneT Sahoo, E Goenaga-Diaz, I G Serebriiskii, et al.
Pageof 7