PuSH - Publication Server of Helmholtz Zentrum München

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1.
Reijnders, M.R.* et al.: PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature. J. Med. Genet. 55, 104-113 (2017)
2.
Tapper, W.* et al.: Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms. Nat. Commun. 6:6691 (2015)
3.
Wilson, N.K.* et al.: Combined single-cell functional and gene expression analysis resolves heterogeneity within stem cell populations. Cell Stem Cell 16, 712-724 (2015)
4.
Jones, A.V.* et al.: The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms. Blood 115, 4517-4523 (2010)