Lenoir GM - Search Results

1

[Familial medullary thyroid cancer. Contribution of genealogy and genetics to the study of two families].

Houdent C, Avronsart B, Dubuisson M, Ozenne G, Testard J, Calmettes C, Chaventre A, Sobol H, Lenoir GM, Wolf LM. Houdent C, et al. Among authors: lenoir gm. Presse Med. 1990 Mar 31;19(12):549-52. Presse Med. 1990. PMID: 2139215 French.

2

Genetic analysis of 24 French families with multiple endocrine neoplasia type 2A.

Narod SA, Lavoué MF, Morgan K, Calmettes C, Sobol H, Goodfellow PJ, Lenoir GM. Narod SA, et al. Among authors: lenoir gm. Am J Hum Genet. 1992 Sep;51(3):469-77. Am J Hum Genet. 1992. PMID: 1353939 Free PMC article.

3

[Predictive tests for familial medullary cancer of the thyroid].

Lenoir GM, Sobol H. Lenoir GM, et al. Pathol Biol (Paris). 1992 Nov;39(9):921-2. Pathol Biol (Paris). 1992. PMID: 1538934 French. No abstract available.

4

[Heredity and medullary cancer of the thyroid].

Assouline D, Sobol H, Maillet-Vioud M, Schuffenecker I, Narod SA, Lenoir GM. Assouline D, et al. Among authors: lenoir gm. Rev Prat. 1990 Jun 1;40(16):1487-9. Rev Prat. 1990. PMID: 2359949 French. No abstract available.

5

Early detection of hereditary medullary thyroid cancer with polymorphic DNA probes. Groupe d'Etude des Tumeurs a Calcitonine.

Narod SA, Sobol H, Schuffenecker I, Ezekowitz RA, Lenoir GM. Narod SA, et al. Among authors: lenoir gm. Henry Ford Hosp Med J. 1989;37(3-4):106-8. Henry Ford Hosp Med J. 1989. PMID: 2576937 Free article.

6

Genetic screening of endocrine tumour syndromes with DNA probes: the example of medullary thyroid carcinoma.

Sobol H, Narod SA, Assouline D, Lenoir GM. Sobol H, et al. Among authors: lenoir gm. Horm Res. 1989;32(1-3):34-40. doi: 10.1159/000181240. Horm Res. 1989. PMID: 2575577 Review.

7

Hereditary medullary thyroid carcinoma: genetic annalysis of three related syndromes. Groupe d'Etude des Tumeurs a Calcitonine.

Sobol H, Narod SA, Schuffenecker I, Amos C, Ezekowitz RA, Lenoir GM. Sobol H, et al. Among authors: lenoir gm. Henry Ford Hosp Med J. 1989;37(3-4):109-11. Henry Ford Hosp Med J. 1989. PMID: 2576938 Free article.

8

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

9

The gene for MEN 2A is tightly linked to the centromere of chromosome 10.

Narod SA, Sobol H, Schuffenecker I, Lavoué MF, Lenoir GM. Narod SA, et al. Among authors: lenoir gm. Hum Genet. 1991 Mar;86(5):529-30. doi: 10.1007/BF00194649. Hum Genet. 1991. PMID: 1673115

10

[Genetics of neurofibromatosis: recent progress and prospects].

Maillet-Vioud M, Narod S, Assouline D, Sobol H, Fischer G, Robert JM, Lenoir GM. Maillet-Vioud M, et al. Among authors: lenoir gm. Rev Neurol (Paris). 1991;147(10):644-52. Rev Neurol (Paris). 1991. PMID: 1763253 Review. French.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

389 results

Search Page

Filters