Results
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41.
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A 90 kb DNA deletion associated with neurofibromatosis type 1. [electronic resource] by
- Upadhyaya, M
- Cheryson, A
- Broadhead, W
- Fryer, A
- Shaw, D J
- Huson, S
- Wallace, M R
- Andersen, L B
- Marchuk, D A
- Viskochil, D
Producer: 19910412
In:
Journal of medical genetics vol. 27
Availability: No items available.
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42.
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43.
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44.
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Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhage. [electronic resource] by
- Alberts, M J
- Davis, J P
- Graffagnino, C
- McClenny, C
- Delong, D
- Granger, C
- Herbstreith, M H
- Boteva, K
- Marchuk, D A
- Roses, A D
Producer: 19970603
In:
Annals of neurology vol. 41
Availability: No items available.
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45.
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Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients. [electronic resource] by
- Wallace, M R
- Marchuk, D A
- Andersen, L B
- Letcher, R
- Odeh, H M
- Saulino, A M
- Fountain, J W
- Brereton, A
- Nicholson, J
- Mitchell, A L
Producer: 19900823
In:
Science (New York, N.Y.) vol. 249
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46.
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47.
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cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 gene. [electronic resource] by
- Cawthon, R M
- Andersen, L B
- Buchberg, A M
- Xu, G F
- O'Connell, P
- Viskochil, D
- Weiss, R B
- Wallace, M R
- Marchuk, D A
- Culver, M
Producer: 19910625
In:
Genomics vol. 9
Availability: No items available.
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48.
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cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene product. [electronic resource] by
- Marchuk, D A
- Saulino, A M
- Tavakkol, R
- Swaroop, M
- Wallace, M R
- Andersen, L B
- Mitchell, A L
- Gutmann, D H
- Boguski, M
- Collins, F S
Producer: 19920313
In:
Genomics vol. 11
Availability: No items available.
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49.
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A yeast artificial chromosome contig encompassing the type 1 neurofibromatosis gene. [electronic resource] by
- Marchuk, D A
- Tavakkol, R
- Wallace, M R
- Brownstein, B H
- Taillon-Miller, P
- Fong, C T
- Legius, E
- Andersen, L B
- Glover, T W
- Collins, F S
Producer: 19920828
In:
Genomics vol. 13
Availability: No items available.
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50.
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Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype. [electronic resource] by
- McAllister, K A
- Lennon, F
- Bowles-Biesecker, B
- McKinnon, W C
- Helmbold, E A
- Markel, D S
- Jackson, C E
- Guttmacher, A E
- Pericak-Vance, M A
- Marchuk, D A
Producer: 19950420
In:
Journal of medical genetics vol. 31
Availability: No items available.
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51.
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Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant disease. [electronic resource] by
- Damji, K F
- Gallione, C J
- Allingham, R R
- Slotterbeck, B
- Guttmacher, A E
- Pasyk, K A
- Vance, J M
- Pericak-Vance, M A
- Speer, M C
- Marchuk, D A
Producer: 19980403
In:
Human genetics vol. 102
Availability: No items available.
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52.
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Endoglin, an ancillary TGFbeta receptor, is required for extraembryonic angiogenesis and plays a key role in heart development. [electronic resource] by
- Arthur, H M
- Ure, J
- Smith, A J
- Renforth, G
- Wilson, D I
- Torsney, E
- Charlton, R
- Parums, D V
- Jowett, T
- Marchuk, D A
- Burn, J
- Diamond, A G
Producer: 20000204
In:
Developmental biology vol. 217
Availability: No items available.
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53.
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A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12. [electronic resource] by
- Johnson, D W
- Berg, J N
- Gallione, C J
- McAllister, K A
- Warner, J P
- Helmbold, E A
- Markel, D S
- Jackson, C E
- Porteous, M E
- Marchuk, D A
Producer: 19961023
In:
Genome research vol. 5
Availability: No items available.
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54.
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A locus for cerebral cavernous malformations maps to chromosome 7q in two families. [electronic resource] by
- Marchuk, D A
- Gallione, C J
- Morrison, L A
- Clericuzio, C L
- Hart, B L
- Kosofsky, B E
- Louis, D N
- Gusella, J F
- Davis, L E
- Prenger, V L
Producer: 19960201
In:
Genomics vol. 28
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55.
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Additional glomangioma families link to chromosome 1p: no evidence for genetic heterogeneity. [electronic resource] by
- Calvert, J T
- Burns, S
- Riney, T J
- Sahoo, T
- Orlow, S J
- Nevin, N C
- Haisley-Royster, C
- Prose, N
- Simpson, S A
- Speer, M C
- Marchuk, D A
Producer: 20010322
In:
Human heredity vol. 51
Availability: No items available.
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56.
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Computational and experimental analyses reveal previously undetected coding exons of the KRIT1 (CCM1) gene. [electronic resource] by
- Sahoo, T
- Goenaga-Diaz, E
- Serebriiskii, I G
- Thomas, J W
- Kotova, E
- Cuellar, J G
- Peloquin, J M
- Golemis, E
- Beitinjaneh, F
- Green, E D
- Johnson, E W
- Marchuk, D A
Producer: 20010510
In:
Genomics vol. 71
Availability: No items available.
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57.
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Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2. [electronic resource] by
- Vikkula, M
- Boon, L M
- Carraway, K L
- Calvert, J T
- Diamonti, A J
- Goumnerov, B
- Pasyk, K A
- Marchuk, D A
- Warman, M L
- Cantley, L C
- Mulliken, J B
- Olsen, B R
Producer: 19970203
In:
Cell vol. 87
Availability: No items available.
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58.
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SMAD4 mutations found in unselected HHT patients. [electronic resource] by
- Gallione, C J
- Richards, J A
- Letteboer, T G W
- Rushlow, D
- Prigoda, N L
- Leedom, T P
- Ganguly, A
- Castells, A
- Ploos van Amstel, J K
- Westermann, C J J
- Pyeritz, R E
- Marchuk, D A
Producer: 20061204
In:
Journal of medical genetics vol. 43
Availability: No items available.
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59.
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Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia. [electronic resource] by
- Svenson, I K
- Ashley-Koch, A E
- Gaskell, P C
- Riney, T J
- Cumming, W J
- Kingston, H M
- Hogan, E L
- Boustany, R M
- Vance, J M
- Nance, M A
- Pericak-Vance, M A
- Marchuk, D A
Producer: 20010607
In:
American journal of human genetics vol. 68
Availability: No items available.
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60.
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Allelic and locus heterogeneity in inherited venous malformations. [electronic resource] by
- Calvert, J T
- Riney, T J
- Kontos, C D
- Cha, E H
- Prieto, V G
- Shea, C R
- Berg, J N
- Nevin, N C
- Simpson, S A
- Pasyk, K A
- Speer, M C
- Peters, K G
- Marchuk, D A
Producer: 19990816
In:
Human molecular genetics vol. 8
Availability: No items available.
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