Sobol H - Search Results

1

Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21.

McKay JD, Lesueur F, Jonard L, Pastore A, Williamson J, Hoffman L, Burgess J, Duffield A, Papotti M, Stark M, Sobol H, Maes B, Murat A, Kääriäinen H, Bertholon-Grégoire M, Zini M, Rossing MA, Toubert ME, Bonichon F, Cavarec M, Bernard AM, Boneu A, Leprat F, Haas O, Lasset C, Schlumberger M, Canzian F, Goldgar DE, Romeo G. McKay JD, et al. Among authors: sobol h. Am J Hum Genet. 2001 Aug;69(2):440-6. doi: 10.1086/321979. Epub 2001 Jul 2. Am J Hum Genet. 2001. PMID: 11438887 Free PMC article.

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

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

7

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

8

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.

9

Linkage analysis of 19 French breast cancer families, with five chromosome 17q markers.

Mazoyer S, Lalle P, Narod SA, Bignon YJ, Courjal F, Jamot B, Dutrillaux B, Stoppa-Lyonnett D, Sobol H. Mazoyer S, et al. Among authors: sobol h. Am J Hum Genet. 1993 Apr;52(4):754-60. Am J Hum Genet. 1993. PMID: 8096359 Free PMC article.

10

Familial ovarian carcinoma: pedigree studies and preliminary results from linkage analysis.

Sobol H, Mazoyer S, Smith SA, Lyonnet D, Bignon YJ, Narod SA, Ardoin A, Biron P, Bobin JY, Bremond A, et al. Sobol H, et al. Bull Cancer. 1993 Feb;80(2):121-34. Bull Cancer. 1993. PMID: 8173163

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