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Functional study of a novel single deletion in the TITF1/NKX2.1 homeobox gene that produces congenital hypothyroidism and benign chorea but not pulmonary distress. [electronic resource] by
- Moya, Christian M
- Perez de Nanclares, Guiomar
- Castaño, Luis
- Potau, Neus
- Bilbao, J Ramón
- Carrascosa, Antonio
- Bargadá, María
- Coya, Raquel
- Martul, Pedro
- Vicens-Calvet, Enric
- Santisteban, Pilar
Producer: 20060607
In:
The Journal of clinical endocrinology and metabolism vol. 91
Availability: No items available.
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11.
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p.L571P in the linker domain of rat thyroglobulin causes intracellular retention. [electronic resource] by
- Citterio, Cintia E
- Siffo, Sofia
- Moya, Christian M
- Pio, Mauricio Gomes
- Molina, Maricel F
- Scheps, Karen G
- Rey, Osvaldo A
- Arvan, Peter
- Rivolta, Carina M
- Targovnik, Héctor M
Producer: 20210204
In:
Molecular and cellular endocrinology vol. 505
Availability: No items available.
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12.
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Association study of 69 genes in the ret pathway identifies low-penetrance loci in sporadic medullary thyroid carcinoma. [electronic resource] by
- Ruiz-Llorente, Sergio
- Montero-Conde, Cristina
- Milne, Roger L
- Moya, Christian M
- Cebrián, Arancha
- Letón, Rocío
- Cascón, Alberto
- Mercadillo, Fátima
- Landa, Iñigo
- Borrego, Salud
- Pérez de Nanclares, Guiomar
- Alvarez-Escolá, Cristina
- Díaz-Pérez, José Angel
- Carracedo, Angel
- Urioste, Miguel
- González-Neira, Anna
- Benítez, Javier
- Santisteban, Pilar
- Dopazo, Joaquín
- Ponder, Bruce A
- Robledo, Mercedes
Producer: 20071031
In:
Cancer research vol. 67
Availability: No items available.
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