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2009 | 1 |
2010 | 1 |
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Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma.
Fam Cancer. 2011 Jun;10(2):337-42. doi: 10.1007/s10689-010-9411-0.
Fam Cancer. 2011.
PMID: 21188540
Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene.
Slade I, Stephens P, Douglas J, Barker K, Stebbings L, Abbaszadeh F, Pritchard-Jones K; FACT collaboration; Cole R, Pizer B, Stiller C, Vujanic G, Scott RH, Stratton MR, Rahman N.
Slade I, et al.
J Med Genet. 2010 May;47(5):342-7. doi: 10.1136/jmg.2009.072983. Epub 2009 Nov 30.
J Med Genet. 2010.
PMID: 19948536
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