Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene. Groupe D'etude des Tumeurs à Calcitonine.

Schuffenecker, I; Virally-Monod, M; Brohet, R; Goldgar, D; Conte-Devolx, B; Leclerc, L; Chabre, O; Boneu, A; Caron, J; Houdent, C; Modigliani, E; Rohmer, V; Schlumberger, M; Eng, C; Guillausseau, P J; Lenoir, G M

Schuffenecker, I; Virally-Monod, M; Brohet, R; Goldgar, D; Conte-Devolx, B; Leclerc, L; Chabre, O; Boneu, A; Caron, J; Houdent, C; Modigliani, E; Rohmer, V; Schlumberger, M; Eng, C; Guillausseau, P J; Lenoir, G M.

Affiliation

Schuffenecker I; Laboratoire de Génétique, Hôpital Edouard Herriot, Lyon, France.

J Clin Endocrinol Metab ; 83(2): 487-91, 1998 Feb.

Article in En | MEDLINE | ID: mdl-9467562

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Collection: 01-internacional Database: MEDLINE Main subject: Codon / Proto-Oncogene Proteins / Receptor Protein-Tyrosine Kinases / Multiple Endocrine Neoplasia Type 2a / Penetrance / Drosophila Proteins / Hyperparathyroidism / Mutation Type of study: Etiology_studies / Risk_factors_studies Limits: Adult / Humans / Middle aged Language: En Journal: J Clin Endocrinol Metab Year: 1998 Document type: Article Affiliation country: Francia Country of publication: Estados Unidos

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