Cited by

• [Forms of congenital poikiloderma].

  WODNIANSKY P. WODNIANSKY P. Arch Klin Exp Dermatol. 1957;205(4):331-42. Arch Klin Exp Dermatol. 1957. PMID: 13522016 German. No abstract available.
• Kindler'S syndrome: a case series of three Indian children.

  Ghosh SK, Bandyopadhyay D, Das J, Chatterjee G, Sarkar S. Ghosh SK, et al. Indian J Dermatol. 2010 Oct;55(4):393-6. doi: 10.4103/0019-5154.74568. Indian J Dermatol. 2010. PMID: 21430900 Free PMC article.
• Phylogenetic analysis of kindlins suggests subfunctionalization of an ancestral unduplicated kindlin into three paralogs in vertebrates.

  Khan AA, Janke A, Shimokawa T, Zhang H. Khan AA, et al. Evol Bioinform Online. 2011 Mar 22;7:7-19. doi: 10.4137/EBO.S6179. Evol Bioinform Online. 2011. PMID: 21487533 Free PMC article.
• Kindler syndrome and periodontal disease: review of the literature and a 12-year follow-up case.

  Wiebe CB, Petricca G, Häkkinen L, Jiang G, Wu C, Larjava HS. Wiebe CB, et al. J Periodontol. 2008 May;79(5):961-6. doi: 10.1902/jop.2008.070167. J Periodontol. 2008. PMID: 18454678 Free PMC article. Review.
• Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.

  Mercier S, Küry S, Salort-Campana E, Magot A, Agbim U, Besnard T, Bodak N, Bou-Hanna C, Bréhéret F, Brunelle P, Caillon F, Chabrol B, Cormier-Daire V, David A, Eymard B, Faivre L, Figarella-Branger D, Fleurence E, Ganapathi M, Gherardi R, Goldenberg A, Hamel A, Igual J, Irvine AD, Israël-Biet D, Kannengiesser C, Laboisse C, Le Caignec C, Mahé JY, Mallet S, MacGowan S, McAleer MA, McLean I, Méni C, Munnich A, Mussini JM, Nagy PL, Odel J, O'Regan GM, Péréon Y, Perrier J, Piard J, Puzenat E, Sampson JB, Smith F, Soufir N, Tanji K, Thauvin C, Ulane C, Watson RM, Khumalo NP, Mayosi BM, Barbarot S, Bézieau S. Mercier S, et al. Orphanet J Rare Dis. 2015 Oct 15;10:135. doi: 10.1186/s13023-015-0352-4. Orphanet J Rare Dis. 2015. PMID: 26471370 Free PMC article.