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| | NEJM -- Familial Forms of Thyroid Dysgenesis among Infants with Congenital Hypothyroidism |
 | | Castanet, M., Park, S.-M., Smith, A., Bost, M., Leger, J., Lyonnet, S., Pelet, A., Czernichow, P., Chatterjee, K., Polak, M. A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate. |
 | | Leger, J., Marinovic, D., Garel, C., Bonaiti-Pellie, C., Polak, M., Czernichow, P. Thyroid Developmental Anomalies in First Degree Relatives of Children with Congenital Hypothyroidism. |
 | | Castanet, M., Polak, M., Bonaïti-Pellié, C., Lyonnet, S., Czernichow, P., Léger, J. Nineteen Years of National Screening for Congenital Hypothyroidism: Familial Cases with Thyroid Dysgenesis Suggest the Involvement of Genetic Factors. |
| content.nejm.org /cgi/content/short/343/6/441?query=nextarrow (441 words) |
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