Hasil Pencarian - Armstrong Linlea

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  1. 1
    Lynch syndrome-chasing a better ascertainment rate in British Columbia

    Lynch syndrome-chasing a better ascertainment rate in British Columbia oleh Cremin Carol, Bashash Morteza, Armstrong Linlea, Gill Sharlene, Huntsman David, Bajdik Chris

    Diterbitkan 2010-05-01
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  2. 2
    Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1

    Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1 oleh Gutowski Nicholas J, Pott Jan WR, Traboulsi Elias I, Yazdani Ahmad, Hunter David G, Geraghty Michael T, Lyons Christopher, Armstrong Linlea, Fredrick Douglas, Dragan Laryssa, Andrews Caroline, Chan Wai-Man, Ellard Sian, Young Elizabeth, Hanisch Frank, Koc Feray, Schnall Bruce, Engle Elizabeth C

    Diterbitkan 2007-05-01
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  3. 3
    Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization

    Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization oleh Li H Irene, Lemyre Emmanuelle, Langlois Sylvie, Gibson William T, Flibotte Stephane, Delaney Allen D, Chai David, Chan Susanna, Boerkoel Cornelius, Birch Patricia, Baross Agnes, Armstrong Linlea, Arbour Laura, Adam Shelin, Friedman JM, MacLeod Patrick, Mathers Joan, Michaud Jacques L, McGillivray Barbara C, Patel Millan S, Qian Hong, Rouleau Guy A, Van Allen Margot I, Yong Siu-Li, Zahir Farah R, Eydoux Patrice, Marra Marco A

    Diterbitkan 2009-11-01
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