Detail Nature Genetics vol. 44 no. 06 (Jun. 2012) Bibliografi Bahasa: (EN )    ISSN: 1061-4036    Year:: 2012    Bulan: 06    Edisi: Jun 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 The Pediatric Cancer Genome Project, halaman 619–622 Exome sequencing and the genetic basis of complex traits, halaman 623–630 Extremely low-coverage sequencing and imputation increases power for genome-wide association studies, halaman 631–635 Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype, halaman 636–638 Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome, halaman 639–641 Detectable clonal mosaicism from birth to old age and its relationship to cancer, halaman 642–650 Detectable clonal mosaicism and its relationship to aging and cancer, halaman 651–658 A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance, halaman 659–669 Meta-analysis identifies six new susceptibility loci for atrial fibrillation, halaman 670–675 Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo, halaman 676–680 A genome-wide association study identifies susceptibility loci for Wilms tumor, halaman 681–684 Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer, halaman 685–689 Exome sequencing of liver fluke–associated cholangiocarcinoma, halaman 690–693 Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma, halaman 694–698 Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1, halaman 699–703 Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration, halaman 704–708 Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1, halaman 709–713 CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms, halaman 714–719 Parallel domestication of the Shattering1 genes in cereals, halaman 720–724 A model-based approach for analysis of spatial structure in genetic data, halaman 725–731  Edit Artikel Lihat Sejarah Pengadaan  Konversi Metadata   Kembali

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