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Journal Abstract Search

123 related items for PubMed ID: 15083698

  • 1. Total anonychia congenita: a rare heterogeneic disorder.
    Ozdemir O, Tiftikcioglu YO, Karaaslan O, Ozdemir R, Kocer U.
    Genet Couns; 2004; 15(1):43-6. PubMed ID: 15083698
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  • 2. Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?
    Teebi AS, Kaurah P.
    Am J Med Genet; 1996 Dec 18; 66(3):257-60. PubMed ID: 8985482
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  • 3. Anonychia Congenita - Rare Inheritance of a Rare Disorder.
    Vasudha J, Jalees F, S P, Raj VA, Tauseef KM.
    J Assoc Physicians India; 2022 Dec 18; 69(12):11-12. PubMed ID: 35057601
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  • 4. Anonychia congenita in different generations of a single Saudi family.
    Bin Nooh DM, Hegazi TM, Bukhari IA.
    Saudi Med J; 2020 Feb 18; 41(2):195-198. PubMed ID: 32020155
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  • 5. The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia.
    Blaydon DC, Ishii Y, O'Toole EA, Unsworth HC, Teh MT, Rüschendorf F, Sinclair C, Hopsu-Havu VK, Tidman N, Moss C, Watson R, de Berker D, Wajid M, Christiano AM, Kelsell DP.
    Nat Genet; 2006 Nov 18; 38(11):1245-7. PubMed ID: 17041604
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  • 6. Anonychia associated with ectrodactyly syndrome: a case report.
    Patiroğlu T, Hasanoğlu E.
    Turk J Pediatr; 1989 Nov 18; 31(3):249-52. PubMed ID: 2485992
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  • 14. Congenital malalignment of great toenails in two sets of monozygotic twins.
    Barth JH, Dawber RP, Ashton RE, Baran R.
    Arch Dermatol; 1986 Apr 18; 122(4):379-80. PubMed ID: 3954405
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  • 15. Congenital brachydactyly and nail hypoplasia: clue to bone-dependent nail formation.
    Seitz CS, Hamm H.
    Br J Dermatol; 2005 Jun 18; 152(6):1339-42. PubMed ID: 15949005
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  • 16. Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.
    Bergmann C, Senderek J, Anhuf D, Thiel CT, Ekici AB, Poblete-Gutierrez P, van Steensel M, Seelow D, Nürnberg G, Schild HH, Nürnberg P, Reis A, Frank J, Zerres K.
    Am J Hum Genet; 2006 Dec 18; 79(6):1105-9. PubMed ID: 17186469
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