These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 11030770)

  • 1. Isolated congenital nail dysplasia: a new autosomal dominant condition.
    Hamm H; Karl S; Bröcker EB
    Arch Dermatol; 2000 Oct; 136(10):1239-43. PubMed ID: 11030770
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Hereditary hypodontia and onychorrhexis of the fingernails and toenail koilonychia: Witkop's tooth-and nail syndrome.
    Zabawski EJ; Cohen JB
    Dermatol Online J; 1999 May; 5(1):3. PubMed ID: 10673446
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Epidermal hamartoma presenting as longitudinal pachyleukonychia: a new nail genodermatosis.
    Moulin G; Baran R; Perrin C
    J Am Acad Dermatol; 1996 Nov; 35(5 Pt 1):675-7. PubMed ID: 8912559
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary brachydactyly with nail dysplasia.
    Schott GD
    J Med Genet; 1978 Apr; 15(2):119-22. PubMed ID: 641944
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Sub-total hereditary leukonychia, histopathological and electron microscopy study of "milky" nails].
    Marcilly MC; Balme B; Haftek M; Wolf F; Grezard P; Berard F; Perrot H
    Ann Dermatol Venereol; 2003 Jan; 130(1 Pt 1):50-4. PubMed ID: 12605159
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia.
    Propping P; Zerres K
    Am J Med Genet; 1993 Mar; 45(5):642-8. PubMed ID: 8456838
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of two novel mutations in the
    Shen S; Shao M; Keyal U; Wang X; Li M; Zhang G
    Mol Med Rep; 2021 Jun; 23(6):. PubMed ID: 33786625
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetics of human isolated hereditary nail disorders.
    Khan S; Basit S; Habib R; Kamal A; Muhammad N; Ahmad W
    Br J Dermatol; 2015 Oct; 173(4):922-9. PubMed ID: 26149975
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New autosomal dominant syndrome resembling craniofrontonasal dysplasia.
    Teebi AS
    Am J Med Genet; 1987 Nov; 28(3):581-91. PubMed ID: 3425628
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a large Iranian kindred.
    Mohammadi-Asl J; Pourreza MR; Mohammadi A; Eskandari A; Mozafar-Jalali S; Tabatabaiefar MA
    J Dermatol Sci; 2017 Oct; 88(1):134-138. PubMed ID: 28545862
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial severe twenty-nail dystrophy.
    Arias AM; Yung CW; Rendler S; Soltani K; Lorincz AL
    J Am Acad Dermatol; 1982 Sep; 7(3):349-52. PubMed ID: 7130495
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital onychodysplasia of the index finger presenting as a congenital bifid nail.
    Crowe D; DiSano K
    Dermatol Online J; 2014 Nov; 20(11):. PubMed ID: 25419756
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. A case report of twenty-nail dystrophy.
    Ohta Y; Katsuoka K
    J Dermatol; 1997 Jan; 24(1):60-2. PubMed ID: 9046745
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial koilonychia.
    Gao XH; Li X; Zhao Y; Wang Y; Chen HD
    Int J Dermatol; 2001 Apr; 40(4):290-1. PubMed ID: 11454091
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant trait.
    Tolmie JL; Wilcox DE; McWilliam R; Assindi A; Stephenson JB
    J Med Genet; 1988 Nov; 25(11):754-7. PubMed ID: 2976839
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prevalence, severity and clinical features of psoriasis in fingernails and toenails in adult patients: Italian experience.
    Brazzelli V; Carugno A; Alborghetti A; Grasso V; Cananzi R; Fornara L; De Silvestri A; Borroni G
    J Eur Acad Dermatol Venereol; 2012 Nov; 26(11):1354-9. PubMed ID: 21973119
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polydactyly, conical teeth, nail dysplasia, and short limbs: a new autosomal dominant malformation syndrome.
    Curry CJ; Hall BD
    Birth Defects Orig Artic Ser; 1979; 15(5B):253-63. PubMed ID: 526581
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.