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Journal Abstract Search

309 related items for PubMed ID: 20409997

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  • 4. A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
    Tariq M, Chishti MS, Ali G, Ahmad W.
    Ann Hum Genet; 2008 Jan; 72(Pt 1):19-25. PubMed ID: 18184143
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  • 5. Mutations in the keratin 85 (KRT85/hHb5) gene underlie pure hair and nail ectodermal dysplasia.
    Shimomura Y, Wajid M, Kurban M, Sato N, Christiano AM.
    J Invest Dermatol; 2010 Mar; 130(3):892-5. PubMed ID: 19865094
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  • 6. Autosomal recessive transmission of a rare KRT74 variant causes hair and nail ectodermal dysplasia: allelism with dominant woolly hair/hypotrichosis.
    Raykova D, Klar J, Azhar A, Khan TN, Malik NA, Iqbal M, Tariq M, Baig SM, Dahl N.
    PLoS One; 2014 Mar; 9(4):e93607. PubMed ID: 24714551
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  • 8. Molecular genetic analysis of consanguineous Pakistani families with autosomal recessive hypohidrotic ectodermal dysplasia.
    Bibi N, Ahmad S, Ahmad W, Naeem M.
    Australas J Dermatol; 2011 Feb; 52(1):37-42. PubMed ID: 21332691
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  • 10. Mutation in the HPGD gene encoding NAD+ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC).
    Tariq M, Azeem Z, Ali G, Chishti MS, Ahmad W.
    J Med Genet; 2009 Jan; 46(1):14-20. PubMed ID: 18805827
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  • 11. Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12-q21.2.
    Naeem M, Jelani M, Lee K, Ali G, Chishti MS, Wali A, Gul A, John P, Hassan MJ, Leal SM, Ahmad W.
    Br J Dermatol; 2006 Dec; 155(6):1184-90. PubMed ID: 17107387
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  • 13. Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees.
    Basit S, Wali A, Aziz A, Muhammad N, Jelani M, Ahmad W.
    Clin Genet; 2011 Mar; 79(3):273-81. PubMed ID: 20528890
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  • 16. Novel mutations in the gene HOXC13 underlying pure hair and nail ectodermal dysplasia in consanguineous families.
    Ali RH, Habib R, Ud-Din N, Khan MN, Ansar M, Ahmad W.
    Br J Dermatol; 2013 Aug; 169(2):478-80. PubMed ID: 23461661
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  • 18. A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31.
    Habib R, Ansar M, Mattheisen M, Shahid M, Ali G, Ahmad W, Betz RC.
    PLoS One; 2015 Aug; 10(6):e0129811. PubMed ID: 26115030
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  • 19. Hereditary 'white nails': a genetic and structural study.
    Norgett EE, Wolf F, Balme B, Leigh IM, Perrot H, Kelsell DP, Haftek M.
    Br J Dermatol; 2004 Jul; 151(1):65-72. PubMed ID: 15270873
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  • 20. Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia.
    Azeem Z, Naqvi SK, Ansar M, Wali A, Naveed AK, Ali G, Hassan MJ, Tariq M, Basit S, Ahmad W.
    Arch Dermatol Res; 2009 Sep; 301(8):625-9. PubMed ID: 19551394
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