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Mendelian diseases among Roman Jews: implications for the origins of disease alleles. [electronic resource] by
- Oddoux, C
- Guillen-Navarro, E
- Ditivoli, C
- Dicave, E
- Cilio, M R
- Clayton, C M
- Nelson, H
- Sarafoglou, K
- McCain, N
- Peretz, H
- Seligsohn, U
- Luzzatto, L
- Nafa, K
- Nardi, M
- Karpatkin, M
- Aksentijevich, I
- Kastner, D
- Axelrod, F
- Ostrer, H
Producer: 20000107
In:
The Journal of clinical endocrinology and metabolism vol. 84
Availability: No items available.
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The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor. [electronic resource] by
- Bernal, S
- Alías, L
- Barceló, M J
- Also-Rallo, E
- Martínez-Hernández, R
- Gámez, J
- Guillén-Navarro, E
- Rosell, J
- Hernando, I
- Rodríguez-Alvarez, F J
- Borrego, S
- Millán, J M
- Hernández-Chico, C
- Baiget, M
- Fuentes-Prior, P
- Tizzano, E F
Producer: 20101215
In:
Journal of medical genetics vol. 47
Availability: No items available.
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