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A clinical molecular scanner: the Melanie project. [electronic resource] by
- Hochstrasser, D F
- Appel, R D
- Vargas, R
- Perrier, R
- Vurlod, J F
- Ravier, F
- Pasquali, C
- Funk, M
- Pellegrini, C
- Muller, A F
Producer: 19910701
In:
M.D. computing : computers in medical practice vol. 8
Availability: No items available.
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A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders. [electronic resource] by
- Innes, A M
- Boycott, K M
- Puffenberger, E G
- Redl, D
- MacDonald, I M
- Chudley, A E
- Beaulieu, C
- Perrier, R
- Gillan, T
- Wade, A
- Parboosingh, J S
Producer: 20110217
In:
Clinical genetics vol. 78
Availability: No items available.
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