Results
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1081.
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1082.
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1083.
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1084.
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1085.
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The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy. [electronic resource] by
- MacKenzie, A E
- Korneluk, R G
- Zorzato, F
- Fujii, J
- Phillips, M
- Iles, D
- Wieringa, B
- Leblond, S
- Bailly, J
- Willard, H F
Producer: 19900621
In:
American journal of human genetics vol. 46
Availability: No items available.
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1086.
|
Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population. [electronic resource] by
- Auburger, G
- Diaz, G O
- Capote, R F
- Sanchez, S G
- Perez, M P
- del Cueto, M E
- Meneses, M G
- Farrall, M
- Williamson, R
- Chamberlain, S
Producer: 19900621
In:
American journal of human genetics vol. 46
Availability: No items available.
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1087.
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1088.
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1089.
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1090.
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1091.
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1092.
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1093.
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1094.
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1095.
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1096.
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1097.
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1098.
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1099.
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1100.
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