-
1
-
-
0001251788
-
Association of pheochromocytoma with carcinoma of the thyroid gland
-
Sipple JH: Association of pheochromocytoma with carcinoma of the thyroid gland. Am J Med 31:163-166, 1961
-
(1961)
Am J Med
, vol.31
, pp. 163-166
-
-
Sipple, J.H.1
-
2
-
-
0020378747
-
Age-related probability of development of hereditary medullary thyroid carcinoma
-
Gagel RF, Jackson CE, Block MA, et al: Age-related probability of development of hereditary medullary thyroid carcinoma. J Pediatr 101:941-946, 1982
-
(1982)
J Pediatr
, vol.101
, pp. 941-946
-
-
Gagel, R.F.1
Jackson, C.E.2
Block, M.A.3
-
3
-
-
0023009002
-
Results of early thyroidectomy for medullary carcinoma in children with multiple endocrine neoplasia type 2
-
Telander RL, Zimmerman D, Van Heerden JA, et al: Results of early thyroidectomy for medullary carcinoma in children with multiple endocrine neoplasia type 2. J Pediatr Surg 21:1190-1194, 1986
-
(1986)
J Pediatr Surg
, vol.21
, pp. 1190-1194
-
-
Telander, R.L.1
Zimmerman, D.2
Van Heerden, J.A.3
-
4
-
-
0024949835
-
Results of a screening program for multiple endocrine neoplasia type 2A
-
Shimotake T, Iwai N, Yanagihara J, et al: Results of a screening program for multiple endocrine neoplasia type 2A. Henry Ford Hosp Med J 37:124-126, 1989
-
(1989)
Henry Ford Hosp Med J
, vol.37
, pp. 124-126
-
-
Shimotake, T.1
Iwai, N.2
Yanagihara, J.3
-
5
-
-
0023229266
-
A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10
-
Mathew CGP, Chin KS, Easton DR, et al: A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10. Nature 328:527-528, 1987
-
(1987)
Nature
, vol.328
, pp. 527-528
-
-
Mathew, C.G.P.1
Chin, K.S.2
Easton, D.R.3
-
6
-
-
0024283881
-
Isolation and mapping of a plymorphic DNA sequence pMCK2 on chromosome 10 [D10S15]
-
Nakamura Y, Carlson M, Krapcho K, et al: Isolation and mapping of a plymorphic DNA sequence pMCK2 on chromosome 10 [D10S15]. Nucleic Acids Res 16:374-376, 1988
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 374-376
-
-
Nakamura, Y.1
Carlson, M.2
Krapcho, K.3
-
7
-
-
0026588042
-
Prediction of affected MEN2A gene carriers by DNA linkage analysis for early total thyroidectomy
-
Shimotake T, Iwai N, Yanagihara J, et al: Prediction of affected MEN2A gene carriers by DNA linkage analysis for early total thyroidectomy. J Pediatr Surg 27:444-446, 1992
-
(1992)
J Pediatr Surg
, vol.27
, pp. 444-446
-
-
Shimotake, T.1
Iwai, N.2
Yanagihara, J.3
-
8
-
-
0024208663
-
Cloning and expression of the ret proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains
-
Takahashi M, Buma Y, Iwamoto T, et al: Cloning and expression of the ret proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains. Oncogene 3:571-578, 1988
-
(1988)
Oncogene
, vol.3
, pp. 571-578
-
-
Takahashi, M.1
Buma, Y.2
Iwamoto, T.3
-
9
-
-
0027231568
-
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan LM, Kwok JB, Healey CS, et al: Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363:458-460, 1993
-
(1993)
Nature
, vol.363
, pp. 458-460
-
-
Mulligan, L.M.1
Kwok, J.B.2
Healey, C.S.3
-
10
-
-
0025899162
-
Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients
-
Nishisho I, Nakamura Y, Miyoshi Y, et al: Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. Science 253:665-669, 1991
-
(1991)
Science
, vol.253
, pp. 665-669
-
-
Nishisho, I.1
Nakamura, Y.2
Miyoshi, Y.3
-
11
-
-
0022506980
-
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
-
Friend SH, Bernards R, Rogelj S, et al: A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma. Nature 323:643-646, 1986
-
(1986)
Nature
, vol.323
, pp. 643-646
-
-
Friend, S.H.1
Bernards, R.2
Rogelj, S.3
-
12
-
-
0023858139
-
Risk estimation and screening in families of patients with medullary thyroid carcinoma
-
Ponder BAJ, Ponder MA, Coffey R, et al: Risk estimation and screening in families of patients with medullary thyroid carcinoma. Lancet 1:397-400, 1988
-
(1988)
Lancet
, vol.1
, pp. 397-400
-
-
Ponder, B.A.J.1
Ponder, M.A.2
Coffey, R.3
-
13
-
-
0028061726
-
Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A
-
Wells SA, Chi DD, Toshima K, et al: Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A. Ann Surg 220:237-250, 1994
-
(1994)
Ann Surg
, vol.220
, pp. 237-250
-
-
Wells, S.A.1
Chi, D.D.2
Toshima, K.3
-
14
-
-
0028120882
-
Point mutations affecting the tyrosine kinase domains of the RET proto-oncogene in Hirschsprung's disease
-
Romeo F, Rochetto P, Luo Y, et al: Point mutations affecting the tyrosine kinase domains of the RET proto-oncogene in Hirschsprung's disease. Nature 367:377-378, 1994
-
(1994)
Nature
, vol.367
, pp. 377-378
-
-
Romeo, F.1
Rochetto, P.2
Luo, Y.3
-
15
-
-
0026602124
-
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
-
Tassabehji M, Read AP, Newton VE, et al: Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene. Nature 355:635-636, 1992
-
(1992)
Nature
, vol.355
, pp. 635-636
-
-
Tassabehji, M.1
Read, A.P.2
Newton, V.E.3
-
16
-
-
0028227569
-
Auditory brainstem response in children with total intestinal aganglionosis
-
Shimotake T, Iwai N: Auditory brainstem response in children with total intestinal aganglionosis. Lancet 343:1362, 1994
-
(1994)
Lancet
, vol.343
, pp. 1362
-
-
Shimotake, T.1
Iwai, N.2
-
17
-
-
0028618372
-
A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease
-
Puffenberger EG, Hosoda K, Washington SS, et al: A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease. Cell 79:1257-1266, 1995
-
(1995)
Cell
, vol.79
, pp. 1257-1266
-
-
Puffenberger, E.G.1
Hosoda, K.2
Washington, S.S.3
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