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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 PJ, Lenoir GM. Schuffenecker I, et al. Among authors: lenoir gm. J Clin Endocrinol Metab. 1998 Feb;83(2):487-91. doi: 10.1210/jcem.83.2.4529. J Clin Endocrinol Metab. 1998. PMID: 9467562
RET proto-oncogene mutations in French MEN 2A and FMTC families.
Schuffenecker I, Billaud M, Calender A, Chambe B, Ginet N, Calmettes C, Modigliani E, Lenoir GM. Schuffenecker I, et al. Among authors: lenoir gm. Hum Mol Genet. 1994 Nov;3(11):1939-43. doi: 10.1093/hmg/3.11.1939. Hum Mol Genet. 1994. PMID: 7874109
The genetics of multiple endocrine neoplasia (MEN).
Calender A, Schuffenecker I, Lenoir GM. Calender A, et al. Among authors: lenoir gm. Horm Res. 1992;38 Suppl 2:16-23. doi: 10.1159/000182587. Horm Res. 1992. PMID: 1363412 Review.
Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine.
Schuffenecker I, Ginet N, Goldgar D, Eng C, Chambe B, Boneu A, Houdent C, Pallo D, Schlumberger M, Thivolet C, Lenoir GM. Schuffenecker I, et al. Among authors: lenoir gm. Am J Hum Genet. 1997 Jan;60(1):233-7. Am J Hum Genet. 1997. PMID: 8981969 Free PMC article. No abstract available.
389 results