Sobol H - Search Results

1

[Hereditary predisposition for cancer of the breast and the ovary].

Lalle P, Stoppa-Lyonnet D, Mazoyer S, Rio P, Girodet C, Hardouin A, Narod SA, Sobol H, Bignon YJ. Lalle P, et al. Among authors: sobol h. Bull Cancer. 1993 Oct;80(10):857-65. Bull Cancer. 1993. PMID: 8204923 French.

2

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

3

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.

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

[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.

7

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

8

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

9

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. Horm Res. 1989;32(1-3):34-40. doi: 10.1159/000181240. Horm Res. 1989. PMID: 2575577 Review.

10

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: sobol h. Henry Ford Hosp Med J. 1989;37(3-4):106-8. Henry Ford Hosp Med J. 1989. PMID: 2576937 Free article.

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