B. Chambe

RET proto-oncogene mutations in French MEN 2A and FMTC families.

G. Lenoir, N. Ginet, I. Schuffenecker, 1994, Human molecular genetics.

Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein

C. Béroud, G. Lenoir, C. Vercherat, 2002, Human mutation.

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.

G M Lenoir, C Eng, C. Eng, 1997, American journal of human genetics.

Pituitary disease in MEN type 1 (MEN1): data from the France-Belgium MEN1 multicenter study.

G. Sassolas, B. Vergès, A. Beckers, 2002, The Journal of clinical endocrinology and metabolism.

Pituitary Disease in MEN Type 1 ( MEN 1 ) : Data from the France-Belgium MEN 1

G. Sassolas, B. Vergès, A. Beckers, 2002 .

Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma [4]

C. Eng, G. Lenoir, M. Schlumberger, 1997 .

[Analysis of the RET gene and medullary cancer of the thyroid. Contribution to the diagnosis and treatment].

G. Lenoir, I. Schuffenecker, B. Chambe, 1996, Annales d'endocrinologie.