BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

287 related articles for article (PubMed ID: 17107387)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pure hair-nail ectodermal dysplasia maps to chromosome 12p11.1-q21.1 in a consanguineous Pakistani family.
    Naeem M; John P; Ali G; Ahmad W
    Clin Exp Dermatol; 2007 Sep; 32(5):502-5. PubMed ID: 17489990
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 10(6):e0129811. PubMed ID: 26115030
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type.
    Naeem M; Wajid M; Lee K; Leal SM; Ahmad W
    J Med Genet; 2006 Mar; 43(3):274-9. PubMed ID: 16525032
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation.
    Rasool M; Nawaz S; Azhar A; Wajid M; Westermark P; Baig SM; Klar J; Dahl N
    Eur J Dermatol; 2010; 20(4):443-6. PubMed ID: 20409997
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Assignment of the gene for a new hereditary nail disorder, isolated congenital nail dysplasia, to chromosome 17p13.
    Krebsová A; Hamm H; Karl S; Reis A; Hennies HC
    J Invest Dermatol; 2000 Oct; 115(4):664-7. PubMed ID: 10998140
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1-17q25.3.
    Rafiq MA; Ansar M; Pham T; Amin-ud-Din M; Anwar M; Haque S; Chahrour MH; Yan K; Leal SM; Ahmad W
    Clin Genet; 2004 Jul; 66(1):73-8. PubMed ID: 15200512
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1.
    Rafiq MA; Faiyaz-Ul-Haque M; Ud Din MA; Malik S; Sohail M; Anwar M; Haque S; Paterson AD; Tsui LC; Ahmad W
    J Invest Dermatol; 2005 Feb; 124(2):338-42. PubMed ID: 15675952
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia.
    Naeem M; Muhammad D; Ahmad W
    Br J Dermatol; 2005 Jul; 153(1):46-50. PubMed ID: 16029325
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Refined mapping of Naegeli-Franceschetti- Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genes.
    Sprecher E; Itin P; Whittock NV; McGrath JA; Meyer R; DiGiovanna JJ; Bale SJ; Uitto J; Richard G
    J Invest Dermatol; 2002 Sep; 119(3):692-8. PubMed ID: 12230514
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3.
    Tariq M; Khan MN; Ahmad W
    Hum Genet; 2009 May; 125(4):421-9. PubMed ID: 19221800
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A homozygous frameshift mutation in the HOXC13 gene underlies pure hair and nail ectodermal dysplasia in a Syrian family.
    Farooq M; Kurban M; Fujimoto A; Fujikawa H; Abbas O; Nemer G; Saliba J; Sleiman R; Tofaili M; Kibbi AG; Ito M; Shimomura Y
    Hum Mutat; 2013 Apr; 34(4):578-81. PubMed ID: 23315978
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clouston syndrome (hidrotic ectodermal dysplasia) is not linked to keratin gene clusters on chromosomes 12 and 17.
    Hayflick SJ; Taylor T; McKinnon W; Guttmacher AE; Litt M; Zonana J
    J Invest Dermatol; 1996 Jul; 107(1):11-4. PubMed ID: 8752831
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2.
    Celebi JT; Tanzi EL; Yao YJ; Michael EJ; Peacocke M
    J Invest Dermatol; 1999 Nov; 113(5):848-50. PubMed ID: 10571744
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21.
    Whittock NV; Coleman CM; McLean WH; Ashton GH; Acland KM; Eady RA; McGrath JA
    J Invest Dermatol; 2000 Oct; 115(4):694-8. PubMed ID: 10998145
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 9(4):e93607. PubMed ID: 24714551
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.