Results
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8275.
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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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8276.
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