Results
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61.
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Central nervous system serotonin function and cardiovascular responses to stress. [electronic resource] by
- Williams, R B
- Marchuk, D A
- Gadde, K M
- Barefoot, J C
- Grichnik, K
- Helms, M J
- Kuhn, C M
- Lewis, J G
- Schanberg, S M
- Stafford-Smith, M
- Suarez, E C
- Clary, G L
- Svenson, I K
- Siegler, I C
Producer: 20010726
In:
Psychosomatic medicine vol. 63
Availability: No items available.
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62.
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Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia. [electronic resource] by
- Ashley-Koch, A
- Bonner, E R
- Gaskell, P C
- West, S G
- Tim, R
- Wolpert, C M
- Jones, R
- Farrell, C D
- Nance, M
- Svenson, I K
- Marchuk, D A
- Boustany, R M
- Vance, J M
- Scott, W K
- Pericak-Vance, M A
Producer: 20010920
In:
Neurogenetics vol. 3
Availability: No items available.
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63.
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Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2. [electronic resource] by
- Johnson, D W
- Berg, J N
- Baldwin, M A
- Gallione, C J
- Marondel, I
- Yoon, S J
- Stenzel, T T
- Speer, M
- Pericak-Vance, M A
- Diamond, A
- Guttmacher, A E
- Jackson, C E
- Attisano, L
- Kucherlapati, R
- Porteous, M E
- Marchuk, D A
Producer: 19960716
In:
Nature genetics vol. 13
Availability: No items available.
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64.
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Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig. [electronic resource] by
- Johnson, E W
- Iyer, L M
- Rich, S S
- Orr, H T
- Gil-Nagel, A
- Kurth, J H
- Zabramski, J M
- Marchuk, D A
- Weissenbach, J
- Clericuzio, C L
- Davis, L E
- Hart, B L
- Gusella, J F
- Kosofsky, B E
- Louis, D N
- Morrison, L A
- Green, E D
- Weber, J L
Producer: 19970305
In:
Genome research vol. 5
Availability: No items available.
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65.
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Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles. [electronic resource] by
- Gallione, C J
- Klaus, D J
- Yeh, E Y
- Stenzel, T T
- Xue, Y
- Anthony, K B
- McAllister, K A
- Baldwin, M A
- Berg, J N
- Lux, A
- Smith, J D
- Vary, C P
- Craigen, W J
- Westermann, C J
- Warner, M L
- Miller, Y E
- Jackson, C E
- Guttmacher, A E
- Marchuk, D A
Producer: 19980604
In:
Human mutation vol. 11
Availability: No items available.
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66.
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Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1). [electronic resource] by
- Sahoo, T
- Johnson, E W
- Thomas, J W
- Kuehl, P M
- Jones, T L
- Dokken, C G
- Touchman, J W
- Gallione, C J
- Lee-Lin, S Q
- Kosofsky, B
- Kurth, J H
- Louis, D N
- Mettler, G
- Morrison, L
- Gil-Nagel, A
- Rich, S S
- Zabramski, J M
- Boguski, M S
- Green, E D
- Marchuk, D A
Producer: 19991214
In:
Human molecular genetics vol. 8
Availability: No items available.
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