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Journal Abstract Search
137 related items for PubMed ID: 23247752
1. [Vohwinkel syndrome. Hearing loss and keratoderma on the hands and feet]. Dippold S, Butsch F, Schopf R, Keilmann A. HNO; 2013 Jul; 61(7):617-9. PubMed ID: 23247752 [Abstract] [Full Text] [Related]
3. A Deletion Mutation of the Connexin 26 (Gjb2) Gene in a Turkish Patient with Vohwinkel Syndrome . Ozturk S, Can I, Eser B, Yazici H. Genet Couns; 2016 Jul; 27(2):187-91. PubMed ID: 29485809 [Abstract] [Full Text] [Related]
4. D66H mutation in GJB2 gene in a Chinese family with classical Vohwinkel syndrome. Qiu Y, Wang Z, Chen N, Song Y, Wang Z, Zhang L. Indian J Dermatol Venereol Leprol; 2012 Jul; 78(5):640-2. PubMed ID: 22960825 [No Abstract] [Full Text] [Related]
5. [Mutation analysis for GJB2 and LOR genes in two patients with Vohwinkel syndrome]. Liu YM, Gao XJ, Tian X, Li XM, Zhang XB. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):203-6. PubMed ID: 23568736 [Abstract] [Full Text] [Related]
13. Hereditary palmoplantar keratoderma and deafness resulting from genetic mutation of Connexin 26. Lee JY, In SI, Kim HJ, Jeong SY, Choung YH, Kim YC. J Korean Med Sci; 2010 Oct; 25(10):1539-42. PubMed ID: 20890442 [Abstract] [Full Text] [Related]
14. A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome. de Zwart-Storm EA, van Geel M, Veysey E, Burge S, Cooper S, Steijlen PM, Martin PE, van Steensel MA. Br J Dermatol; 2011 Jan; 164(1):197-9. PubMed ID: 20854437 [Abstract] [Full Text] [Related]
15. Connecting with connexins. Williams P, Memon A, Sinha T, Fryer A. Australas J Dermatol; 2013 Nov; 54(4):287-9. PubMed ID: 23808595 [Abstract] [Full Text] [Related]
16. Vohwinkel's syndrome in three generations. Solis RR, Diven DG, Trizna Z. J Am Acad Dermatol; 2001 Feb; 44(2 Suppl):376-8. PubMed ID: 11174420 [Abstract] [Full Text] [Related]