432 related articles for article (PubMed ID: 1672289)
1. Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A.
Lairmore TC; Howe JR; Korte JA; Dilley WG; Aine L; Aine E; Wells SA; Donis-Keller H
Genomics; 1991 Jan; 9(1):181-92. PubMed ID: 1672289
[TBL] [Abstract][Full Text] [Related]
2. 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
Genomics; 1990 Oct; 8(2):313-7. PubMed ID: 1979053
[TBL] [Abstract][Full Text] [Related]
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
Am J Hum Genet; 1992 Sep; 51(3):469-77. PubMed ID: 1353939
[TBL] [Abstract][Full Text] [Related]
4. The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10.
Carson NL; Wu JS; Jackson CE; Kidd KK; Simpson NE
Am J Hum Genet; 1990 Dec; 47(6):946-51. PubMed ID: 1978560
[TBL] [Abstract][Full Text] [Related]
5. A new DNA marker (D10S94) very tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus.
Goodfellow PJ; Myers S; Anderson LL; Brooks-Wilson AR; Simpson NE
Am J Hum Genet; 1990 Dec; 47(6):952-6. PubMed ID: 1978561
[TBL] [Abstract][Full Text] [Related]
6. 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
Henry Ford Hosp Med J; 1989; 37(3-4):109-11. PubMed ID: 2576938
[TBL] [Abstract][Full Text] [Related]
7. The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10.
Wu JS; Carson NL; Myers S; Pakstis AJ; Kidd JR; Castiglione CM; Anderson L; Hoyle LS; Genel M; Verdy M
Am J Hum Genet; 1990 Mar; 46(3):624-30. PubMed ID: 1968709
[TBL] [Abstract][Full Text] [Related]
8. Genetics of the multiple endocrine neoplasia type 2B syndrome.
Jackson CE; Norum RA
Henry Ford Hosp Med J; 1992; 40(3-4):232-5. PubMed ID: 1362412
[TBL] [Abstract][Full Text] [Related]
9. A cluster of CpG islands at D10S94, near the locus responsible for multiple endocrine neoplasia type 2A (MEN2A).
Brooks-Wilson AR; Smailus DE; Goodfellow PJ
Genomics; 1992 Jun; 13(2):339-43. PubMed ID: 1351867
[TBL] [Abstract][Full Text] [Related]
10. Genomic and yeast artificial chromosome long-range physical maps linking six loci in 10q11.2 and spanning the multiple endocrine neoplasia type 2A (MEN2A) region.
Brooks-Wilson AR; Lichter JB; Ward DC; Kidd KK; Goodfellow PJ
Genomics; 1993 Sep; 17(3):611-7. PubMed ID: 7902324
[TBL] [Abstract][Full Text] [Related]
11. Low incidence of loss of chromosome 10 in sporadic and hereditary human medullary thyroid carcinoma.
Nelkin BD; Nakamura Y; White RW; de Bustros AC; Herman J; Wells SA; Baylin SB
Cancer Res; 1989 Aug; 49(15):4114-9. PubMed ID: 2568166
[TBL] [Abstract][Full Text] [Related]
12. A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus.
Lichter JB; Wu J; Brooks-Wilson AR; Difillipantonio M; Brewster S; Ward DC; Goodfellow PJ; Kidd KK
Hum Genet; 1993 Jan; 90(5):516-20. PubMed ID: 8094065
[TBL] [Abstract][Full Text] [Related]
13. Improved predictive test for MEN2, using flanking dinucleotide repeats and RFLPs.
Howe JR; Lairmore TC; Mishra SK; Dou S; Veile R; Wells SA; Donis-Keller H
Am J Hum Genet; 1992 Dec; 51(6):1430-42. PubMed ID: 1361102
[TBL] [Abstract][Full Text] [Related]
14. 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
Hum Genet; 1989 Nov; 83(4):353-8. PubMed ID: 2572534
[TBL] [Abstract][Full Text] [Related]
15. Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2.
Gardner E; Papi L; Easton DF; Cummings T; Jackson CE; Kaplan M; Love DR; Mole SE; Moore JK; Mulligan LM
Hum Mol Genet; 1993 Mar; 2(3):241-6. PubMed ID: 8098977
[TBL] [Abstract][Full Text] [Related]
16. Linked markers flanking the gene for multiple endocrine neoplasia type 2A.
Nakamura Y; Mathew CG; Sobol H; Easton DF; Telenius H; Bragg T; Chin K; Clark J; Jones C; Lenoir GM
Genomics; 1989 Aug; 5(2):199-203. PubMed ID: 2571570
[TBL] [Abstract][Full Text] [Related]
17. Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes.
Moley JF; Brother MB; Fong CT; White PS; Baylin SB; Nelkin B; Wells SA; Brodeur GM
Cancer Res; 1992 Feb; 52(4):770-4. PubMed ID: 1346584
[TBL] [Abstract][Full Text] [Related]
18. Genetic screening of endocrine tumour syndromes with DNA probes: the example of medullary thyroid carcinoma.
Sobol H; Narod SA; Assouline D; Lenoir GM
Horm Res; 1989; 32(1-3):34-40. PubMed ID: 2575577
[TBL] [Abstract][Full Text] [Related]
19. Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2.
Mulligan LM; Gardner E; Smith BA; Mathew CG; Ponder BA
Genes Chromosomes Cancer; 1993 Mar; 6(3):166-77. PubMed ID: 7682102
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
