Clinical and molecular analysis of three Mexican families with Pendred's syndrome von GONZALEZ TREVINO, O, KARAMANOGLU ARSEVEN, O, CEBALLOS, C. J, VIVES, V. I, RAMIREZ, R. C, GOMEZ, V. V, MEDEIROS-NETO, G, KOPP, P

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Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene von KOPP, P, ARSEVEN, O. K, SABACAN, L, KOTLAR, T, DUPUIS, J, CAVALIERE, H, SANTOS, C. L. S, JAMESON, J. L, MEDEIROS-NETO, G

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Phenocopies for Deafness and Goiter Development in a Large Inbred Brazilian Kindred with Pendred’s Syndrome Associated with a Novel Mutation in the PDS Gene1 von Kopp, P., Arseven, O. Karamanoglu, Sabacan, L., Kotlar, T., Dupuis, J., Cavaliere, H., Santos, C. L. S., Jameson, J. L., Medeiros-Neto, G.

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Phenocopies for Deafness and Goiter Development in a Large Inbred Brazilian Kindred with Pendred’s Syndrome Associated with a Novel Mutation in the PDS Gene 1 von Kopp, P., Arseven, O. Karamanoglu, Sabacan, L., Kotlar, T., Dupuis, J., Cavaliere, H., Santos, C. L. S., Jameson, J. L., Medeiros-Neto, G.

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Thyrotropin Receptor Mutations in Hyperfunctioning Thyroid Adenomas from Brazil von Nogueira, C R, Kopp, P, Arseven, O K, Santos, C L, Jameson, J L, Medeiros-Neto, G

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Cloning of the cat TSH receptor and evidence against an autoimmune etiology of feline hyperthyroidism von Nguyen, Lynda Q, Arseven, Onur Karamanoglu, Gerber, Hans, Stein, Barbara S, Jameson, J Larry, Kopp, Peter

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Structural Analysis of the Thyrotropin Receptor in Four Patients with Congenital Hypothyroidism Due to Thyroid Hypoplasia von Nogueira, C R, Nguyen, L Q, Coelho-Neto, J R, Arseven, O K, Jameson, J L, Kopp, P, Medeiros-Neto, G A

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