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Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD). [electronic resource] by
- Gilbert, J R
- Stajich, J M
- Wall, S
- Carter, S C
- Qiu, H
- Vance, J M
- Stewart, C S
- Speer, M C
- Pufky, J
- Yamaoka, L H
Producer: 19930809
In:
American journal of human genetics vol. 53
Availability: No items available.
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59.
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Linkage studies in facioscapulohumeral muscular dystrophy (FSHD). [electronic resource] by
- Gilbert, J R
- Stajich, J M
- Speer, M C
- Vance, J M
- Stewart, C S
- Yamaoka, L H
- Samson, F
- Fardeau, M
- Potter, T G
- Roses, A D
Producer: 19920901
In:
American journal of human genetics vol. 51
Availability: No items available.
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60.
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Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17. [electronic resource] by
- Vance, J M
- Nicholson, G A
- Yamaoka, L H
- Stajich, J
- Stewart, C S
- Speer, M C
- Hung, W Y
- Roses, A D
- Barker, D
- Pericak-Vance, M A
Producer: 19890606
In:
Experimental neurology vol. 104
Availability: No items available.
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