-
1
-
-
0001445647
-
Cerebral gigantism in childhood. A syndrome of excessively rapid growth and acromegalic features and a nonprogressive neurologic disorder
-
Sotos JF, Dodge PR, Muirhead D, Crawford JD, Talbot NB. Cerebral gigantism in childhood. A syndrome of excessively rapid growth and acromegalic features and a nonprogressive neurologic disorder.N Engl J Med 1964;271:109-16.
-
(1964)
N Engl J Med
, vol.271
, pp. 109-116
-
-
Sotos, J.F.1
Dodge, P.R.2
Muirhead, D.3
Crawford, J.D.4
Talbot, N.B.5
-
2
-
-
0028078759
-
Sotos syndrome: A study of the diagnostic criteria and natural history
-
Cole TR, Hughes HE. Sotos syndrome: a study of the diagnostic criteria and natural history. J Med Genet 1994;31:20-32. (Pubitemid 24037942)
-
(1994)
Journal of Medical Genetics
, vol.31
, Issue.1
, pp. 20-32
-
-
Cole, T.R.P.1
Hughes, H.E.2
-
3
-
-
18544384537
-
Haploinsufficiency of NSD1 causes Sotos syndrome
-
Kurotaki N, Imaizumi K, Harada N, Masuno M, Kondoh T, Nagai T, et al. Haploinsufficiency of NSD1 causes Sotos syndrome. Nat Genet 2002;30:365-6.
-
(2002)
Nat Genet
, vol.30
, pp. 365-366
-
-
Kurotaki, N.1
Imaizumi, K.2
Harada, N.3
Masuno, M.4
Kondoh, T.5
Nagai, T.6
-
4
-
-
0037238315
-
Familial Sotos syndrome is caused by a novel 1 bp deletion of the NSD1 gene [3]
-
Hoglund P, Kurotaki N, Kytola S, Miyake N, Somer M, Matsumoto N. Familial Sotos syndrome is caused by a novel 1 bp deletion of the NSD1 gene. J Med Genet 2003;40:51-4. (Pubitemid 36115126)
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.1
, pp. 51-54
-
-
Hoglund, P.1
Kurotaki, N.2
Kytola, S.3
Miyake, N.4
Somer, M.5
Matsumoto, N.6
-
6
-
-
0026581535
-
Risk of malignancy in Sotos syndrome
-
Hersh JH, Cole TR, Bloom AS, Bertolone SJ, Hughes HE. Risk of malignancy in Sotos syndrome. J Pediatr 1992;120:572-4.
-
(1992)
J Pediatr
, vol.120
, pp. 572-574
-
-
Hersh, J.H.1
Cole, T.R.2
Bloom, A.S.3
Bertolone, S.J.4
Hughes, H.E.5
-
8
-
-
22244453416
-
A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays
-
DOI 10.1158/0008-5472.CAN-05-0465
-
Nannya Y, Sanada M, Nakazaki K, Hosoya N, Wang L, Hangaishi A, et al. A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. Cancer Res 2005;65:6071-9. (Pubitemid 40994391)
-
(2005)
Cancer Research
, vol.65
, Issue.14
, pp. 6071-6079
-
-
Nannya, Y.1
Sanada, M.2
Nakazaki, K.3
Hosoya, N.4
Wang, L.5
Hangaishi, A.6
Kurokawa, M.7
Chiba, S.8
Bailey, D.K.9
Kennedy, G.C.10
Ogawa, S.11
-
9
-
-
34347229790
-
Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide- polymorphism genotyping microarrays
-
DOI 10.1086/518809
-
Yamamoto G, Nannya Y, Kato M, Sanada M, Levine RL, Kawamata N, et al. Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide- polymorphism genotyping microarrays. Am J Hum Genet 2007;81:114-26. (Pubitemid 47001161)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.1
, pp. 114-126
-
-
Yamamoto, G.1
Nannya, Y.2
Kato, M.3
Sanada, M.4
Levine, R.L.5
Kawamata, N.6
Hangaishi, A.7
Kurokawa, M.8
Chiba, S.9
Gilliland, D.G.10
Koeffler, H.P.11
Ogawa, S.12
-
10
-
-
38949099684
-
Whole-genome profiling of chromosomal aberrations in hepatoblastoma using high-density single-nucleotide polymorphism genotyping microarrays
-
DOI 10.1111/j.1349-7006.2007.00710.x
-
Suzuki M, Kato M, Yuyan C, Takita J, Sanada M, Nannya Y, et al. Wholegenome profiling of chromosomal aberrations in hepatoblastoma using high-density single-nucleotide polymorphism genotyping microarrays. Cancer Sci 2008;99:564-70. (Pubitemid 351228574)
-
(2008)
Cancer Science
, vol.29
, Issue.3
, pp. 564-570
-
-
Suzuki, M.1
Kato, M.2
Yuyan, C.3
Takita, J.4
Sanada, M.5
Nannya, Y.6
Yamamoto, G.7
Takahashi, A.8
Ikeda, H.9
Kuwano, H.10
Ogawa, S.11
Hayashi, Y.12
-
11
-
-
54049118823
-
Oncogenic mutations of ALK kinase in neuroblastoma
-
Chen Y, Takita J, Choi YL, Kato M, Ohira M, Sanada M, et al. Oncogenic mutations of ALK kinase in neuroblastoma. Nature 2008;455:971-4.
-
(2008)
Nature
, vol.455
, pp. 971-974
-
-
Chen, Y.1
Takita, J.2
Choi, Y.L.3
Kato, M.4
Ohira, M.5
Sanada, M.6
-
12
-
-
0036538848
-
Fluorescence in situ hybridization improves cytogenetic results in the analysis of hepatoblastoma
-
DOI 10.1016/S0165-4608(01)00586-6, PII S0165460801005866
-
Sainati L, Leszl A, Surace C, Perilongo G, Rocchi M, Basso G. Fluorescence in situ hybridization improves cytogenetic results in the analysis of hepatoblastoma. Cancer Genet Cytogenet 2002;134:18-20. (Pubitemid 34462103)
-
(2002)
Cancer Genetics and Cytogenetics
, vol.134
, Issue.1
, pp. 18-20
-
-
Sainati, L.1
Leszl, A.2
Surace, C.3
Perilongo, G.4
Rocchi, M.5
Basso, G.6
-
13
-
-
0037130449
-
Mutational spectrum of β-catenin, AXIN1, and AXIN2 in hepatocellular carcinomas and hepatoblastomas
-
DOI 10.1038/sj.onc.1205591
-
Taniguchi K, Roberts LR, Aderca IN, Dong X, Qian C, Murphy LM, et al. Mutational spectrum of beta-catenin, AXIN1, and AXIN2 in hepatocellular carcinomas and hepatoblastomas. Oncogene 2002;21:4863-71. (Pubitemid 34879463)
-
(2002)
Oncogene
, vol.21
, Issue.31
, pp. 4863-4871
-
-
Taniguchi, K.1
Roberts, L.R.2
Aderca, I.N.3
Dong, X.4
Qian, C.5
Murphy, L.M.6
Nagorney, D.M.7
Burgart, L.J.8
Roche, P.C.9
Smith, D.I.10
Ross, J.A.11
Liu, W.12
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