Detail Nature Genetics vol. 44 no. 03 (Mar. 2012) Bibliografi Bahasa: (EN )    ISSN: 1061-4036    Year:: 2012    Bulan: 03    Edisi: Mar 2012     Penerbit: Nature Publishing Group Jenis: Journal - ilmiah internasional [Lihat daftar eksemplar jurnal Nature Genetics] Ketersediaan Perpustakaan FK Nomor Panggil: N12.K.2012.01 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada     Lihat Detail Induk Artikel dalam koleksi ini Differential confounding of rare and common variants in spatially structured populations, halaman 243–246 Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs, halaman 247–250 Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomas, halaman 251–253 Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis, halaman 254–256 Common variants at 11p13 are associated with susceptibility to tuberculosis, halaman 257–259 Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways, halaman 260–268 Genome-wide association study identifies multiple loci influencing human serum metabolite levels, halaman 269–276 Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility, halaman 277–284 Chromosome-scale selective sweeps shape Caenorhabditis elegans genomic diversity, halaman 285–290 Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis, halaman 291–296 Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes, halaman 297–301 Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations, halaman 302–306 Meta-analysis identifies common variants associated with body mass index in east Asians, halaman 307–311 Genome-wide association analysis identifies three new breast cancer susceptibility loci, halaman 312–318 Discovery of common variants associated with low TSH levels and thyroid cancer risk, halaman 319–322 Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma, halaman 323–327 Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke, halaman 328–333 Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis, halaman 334–337 Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus, halaman 338–342 Epigenetic repression of cardiac progenitor gene expression by Ezh2 is required for postnatal cardiac homeostasis, halaman 343–347 Periodic stripe formation by a Turing mechanism operating at growth zones in the mammalian palate, halaman 348–351 Pneumococcal genome sequencing tracks a vaccine escape variant formed through a multi-fragment recombination event, halaman 352–355  Edit Artikel Lihat Sejarah Pengadaan  Konversi Metadata   Kembali

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