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Genetic heterogeneity in neuronal ceroid lipofuscinosis (NCL): evidence that the late-infantile subtype (Jansky-Bielschowsky disease; CLN2) is not an allelic form of the juvenile or infantile subtypes. [electronic resource] by
- Williams, R
- Vesa, J
- Järvelä, I
- McKay, T
- Mitchison, H
- Hellsten, E
- Thompson, A
- Callen, D
- Sutherland, G
- Luna-Battadano, D
Producer: 19931028
In:
American journal of human genetics vol. 53
Availability: No items available.
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Identification of YAC clones for human chromosome 1p32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locus. [electronic resource] by
- Hellsten, E
- Vesa, J
- Heiskanen, M
- Mäkelä, T P
- Järvelä, I
- Cowell, J K
- Mead, S
- Alitalo, K
- Palotie, A
- Peltonen, L
Producer: 19950721
In:
Genomics vol. 25
Availability: No items available.
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