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Familial tumoral calcinosis and hyperostosis-hyperphosphataemia syndrome are different manifestations of the same disease: novel missense mutations in GALNT3.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Genetic heterogeneity for SMARCB1, H3F3A and BRAF in a malignant childhood brain tumour: genetic-pathological correlation.
- Published in:
- Neuropathology & Applied Neurobiology, 2015, v. 41, n. 6, p. 832, doi. 10.1111/nan.12257
- By:
- Publication type:
- Article
Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS.
- Published in:
- Journal of Investigative Dermatology, 2013, v. 133, n. 9, p. 2229, doi. 10.1038/jid.2013.70
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- Publication type:
- Article
Molecular profiling reveals frequent gain of MYCN and anaplasia-specific loss of 4q and 14q in wilms tumor.
- Published in:
- Genes, Chromosomes & Cancer, 2011, v. 50, n. 12, p. 982, doi. 10.1002/gcc.20907
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- Publication type:
- Article
Prognostic classification of relapsing favorable histology Wilms tumor using cDNA microarray expression profiling and support vector machines.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 41, n. 1, p. 65, doi. 10.1002/gcc.20060
- By:
- Publication type:
- Article
Expression profile of wild-type ETV6 in childhood acute leukaemia.
- Published in:
- British Journal of Haematology, 2003, v. 122, n. 1, p. 94, doi. 10.1046/j.1365-2141.2003.04399.x
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- Publication type:
- Article