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Cloning, chromosomal localization, and functional expression of the alpha 1 subunit of the L-type voltage-dependent calcium channel from normal human heart. [electronic resource] by
- Schultz, D
- Mikala, G
- Yatani, A
- Engle, D B
- Iles, D E
- Segers, B
- Sinke, R J
- Weghuis, D O
- Klöckner, U
- Wakamori, M
Producer: 19930806
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 90
Availability: No items available.
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11.
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Multipoint mapping of the central core disease locus. [electronic resource] by
- Schwemmle, S
- Wolff, K
- Palmucci, L M
- Grimm, T
- Lehmann-Horn, F
- Hübner, C
- Hauser, E
- Iles, D E
- MacLennan, D H
- Müller, C R
Producer: 19931022
In:
Genomics vol. 17
Availability: No items available.
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12.
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Localization of the gene encoding the alpha 2/delta-subunits of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families. [electronic resource] by
- Iles, D E
- Lehmann-Horn, F
- Scherer, S W
- Tsui, L C
- Olde Weghuis, D
- Suijkerbuijk, R F
- Heytens, L
- Mikala, G
- Schwartz, A
- Ellis, F R
Producer: 19941130
In:
Human molecular genetics vol. 3
Availability: No items available.
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Genetic mapping of the beta 1- and gamma-subunits of the human skeletal muscle L-type voltage-dependent calcium channel on chromosome 17q and exclusion as candidate genes for malignant hyperthermia susceptibility. [electronic resource] by
- Iles, D E
- Segers, B
- Sengers, R C
- Monsieurs, K
- Heytens, L
- Halsall, P J
- Hopkins, P M
- Ellis, F R
- Hall-Curran, J L
- Stewart, A D
Producer: 19931004
In:
Human molecular genetics vol. 2
Availability: No items available.
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Refined genetic localization for central core disease. [electronic resource] by
- Mulley, J C
- Kozman, H M
- Phillips, H A
- Gedeon, A K
- McCure, J A
- Iles, D E
- Gregg, R G
- Hogan, K
- Couch, F J
- MacLennan, D H
Producer: 19930310
In:
American journal of human genetics vol. 52
Availability: No items available.
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16.
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The G1021A substitution in the RYR1 gene does not cosegregate with malignant hyperthermia susceptibility in a British pedigree. [electronic resource] by
- Adeokun, A M
- West, S P
- Ellis, F R
- Halsall, P J
- Hopkins, P M
- Foroughmand, A M
- Iles, D E
- Robinson, R L
- Stewart, A D
- Curran, J L
Producer: 19970508
In:
American journal of human genetics vol. 60
Availability: No items available.
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17.
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Genetic variation in RYR1 and malignant hyperthermia phenotypes. [electronic resource] by
- Carpenter, D
- Robinson, R L
- Quinnell, R J
- Ringrose, C
- Hogg, M
- Casson, F
- Booms, P
- Iles, D E
- Halsall, P J
- Steele, D S
- Shaw, M-A
- Hopkins, P M
Producer: 20091026
In:
British journal of anaesthesia vol. 103
Availability: No items available.
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Segregation of malignant hyperthermia, central core disease and chromosome 19 markers. [electronic resource] by
- Curran, J L
- Hall, W J
- Halsall, P J
- Hopkins, P M
- Iles, D E
- Markham, A F
- McCall, S H
- Robinson, R L
- West, S P
- Bridges, L R
- Ellis, F R
Producer: 20000106
In:
British journal of anaesthesia vol. 83
Availability: No items available.
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