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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

165 related items for PubMed ID: 27057589

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  • 29. Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.
    Ramprasad VL, Ebenezer ND, Aung T, Rajagopal R, Yong VH, Tuft SJ, Viswanathan D, El-Ashry MF, Liskova P, Tan DT, Bhattacharya SS, Kumaramanickavel G, Vithana EN.
    Hum Mutat; 2007 May; 28(5):522-3. PubMed ID: 17397048
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  • 30. Harboyan syndrome: novel SLC4A11 mutation, clinical manifestations, and outcome of corneal transplantation.
    Tananuvat N, Tananuvat R, Chartapisak W, Mahanupab P, Hokierti C, Srikummool M, Kampuansai J, Intachai W, Olsen B, Ketudat Cairns JR, Kantaputra P.
    J Hum Genet; 2021 Feb; 66(2):193-203. PubMed ID: 32884076
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  • 33. Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.
    Hand CK, Harmon DL, Kennedy SM, FitzSimon JS, Collum LM, Parfrey NA.
    Genomics; 1999 Oct 01; 61(1):1-4. PubMed ID: 10512674
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  • 40. Analysis of SLC4A11, ZEB1, LOXHD1, COL8A2 and TCF4 gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy.
    Tang H, Zhang W, Yan XM, Wang LP, Dong H, Shou T, Lei H, Guo Q.
    Int J Mol Med; 2016 Jun 01; 37(6):1487-500. PubMed ID: 27121161
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