Sobol H - Search Results

1

Genetic heterogeneity of early-onset familial breast cancer.

Sobol H, Mazoyer S, Narod SA, Smith SA, Black DM, Kerbrat P, Jamot B, Solomon E, Ponder BA, Guerin D. Sobol H, et al. Hum Genet. 1992 Jun;89(4):381-3. doi: 10.1007/BF00194307. Hum Genet. 1992. PMID: 1352270

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: sobol h. 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. Among authors: sobol h. Pathol Biol (Paris). 1992 Nov;39(9):921-2. Pathol Biol (Paris). 1992. PMID: 1538934 French. No abstract available.

4

The gene for mannose-binding protein maps to chromosome 10 and is a marker for multiple endocrine neoplasia type 2.

Schuffenecker I, Narod SA, Ezekowitz RA, Sobol H, Feunteun J, Lenoir GM. Schuffenecker I, et al. Among authors: sobol h. Cytogenet Cell Genet. 1991;56(2):99-102. doi: 10.1159/000133058. Cytogenet Cell Genet. 1991. PMID: 1672848

5

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: sobol h. Hum Genet. 1991 Mar;86(5):529-30. doi: 10.1007/BF00194649. Hum Genet. 1991. PMID: 1673115

6

[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: sobol h. Rev Neurol (Paris). 1991;147(10):644-52. Rev Neurol (Paris). 1991. PMID: 1763253 Review. French.

7

Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A.

Norum RA, Lafreniere RG, O'Neal LW, Nikolai TF, Delaney JP, Sisson JC, Sobol H, Lenoir GM, Ponder BA, Willard HF, et al. Norum RA, et al. Among authors: sobol h. Genomics. 1990 Oct;8(2):313-7. doi: 10.1016/0888-7543(90)90287-5. Genomics. 1990. PMID: 1979053 Free article.

8

[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: sobol h. Rev Prat. 1990 Jun 1;40(16):1487-9. Rev Prat. 1990. PMID: 2359949 French. No abstract available.

9

Screening for multiple endocrine neoplasia type 2a with DNA-polymorphism analysis.

Sobol H, Narod SA, Nakamura Y, Boneu A, Calmettes C, Chadenas D, Charpentier G, Chatal JF, Delepine N, Delisle MJ. Sobol H, et al. N Engl J Med. 1989 Oct 12;321(15):996-1001. doi: 10.1056/NEJM198910123211502. N Engl J Med. 1989. PMID: 2571086

10

Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma.

Narod SA, Sobol H, Nakamura Y, Calmettes C, Baulieu JL, Bigorgne JC, Chabrier G, Couette J, de Gennes JL, Duprey J, et al. Narod SA, et al. Among authors: sobol h. Hum Genet. 1989 Nov;83(4):353-8. doi: 10.1007/BF00291380. Hum Genet. 1989. PMID: 2572534

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