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C Houdent

Showing results (41-50 of 46) with videos related to

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Presse Medicale (Paris, France : 1983)|March 31, 1990
[Familial medullary thyroid cancer. Contribution of genealogy and genetics to the study of two families]C Houdent, B Avronsart, M Dubuisson, et al.
Annales D'Endocrinologie|January 1, 1989
[Pituitary adenoma treated with a somatostatin analog]C Houdent, M F Armangau, J M Kuhn, et al.
American Journal of Human Genetics|January 1, 1997
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 CalcitonineI Schuffenecker, N Ginet, D Goldgar, et al.
Clinical Endocrinology|May 1, 1993
Phaeochromocytoma in multiple endocrine neoplasia type 2 A: survey of 100 casesS Casanova, M Rosenberg-Bourgin, D Farkas, et al.
World Journal of Surgery|September 1, 1996
Primary hyperparathyroidism in multiple endocrine neoplasia type IIa: retrospective French multicentric study. Groupe d'Etude des Tumeurs á Calcitonine (GETC, French Calcitonin Tumors Study Group), French Association of Endocrine SurgeonsJ L Kraimps, A Denizot, B Carnaille, et al.
The Journal of Clinical Endocrinology and Metabolism|February 19, 1998
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 CalcitonineI Schuffenecker, M Virally-Monod, R Brohet, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Presse Medicale (Paris, France : 1983)|March 31, 1990
[Familial medullary thyroid cancer. Contribution of genealogy and genetics to the study of two families]C Houdent, B Avronsart, M Dubuisson, et al.
Annales D'Endocrinologie|January 1, 1989
[Pituitary adenoma treated with a somatostatin analog]C Houdent, M F Armangau, J M Kuhn, et al.
American Journal of Human Genetics|January 1, 1997
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 CalcitonineI Schuffenecker, N Ginet, D Goldgar, et al.
Clinical Endocrinology|May 1, 1993
Phaeochromocytoma in multiple endocrine neoplasia type 2 A: survey of 100 casesS Casanova, M Rosenberg-Bourgin, D Farkas, et al.
World Journal of Surgery|September 1, 1996
Primary hyperparathyroidism in multiple endocrine neoplasia type IIa: retrospective French multicentric study. Groupe d'Etude des Tumeurs á Calcitonine (GETC, French Calcitonin Tumors Study Group), French Association of Endocrine SurgeonsJ L Kraimps, A Denizot, B Carnaille, et al.
The Journal of Clinical Endocrinology and Metabolism|February 19, 1998
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 CalcitonineI Schuffenecker, M Virally-Monod, R Brohet, et al.
Pageof 5