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Articles related to 16780467 [Unique ID], provided by the PubMed system
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Gupta N, Phadke SR 
Cutis Laxa Type II and Wrinkly Skin Syndrome: Distinct Phenotypes. [Journal Article]
Pediatr Dermatol 2006 May-Jun; 23(3):225-30.
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Morava E, Wopereis S, Coucke P, et al. 
Defective protein glycosylation in patients with cutis laxa syndrome. [Case Reports, Journal Article]
Eur J Hum Genet 2005 Apr; 13(4):414-21.
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Nanda A, Alsaleh QA, Al-Sabah H, et al. 
Gerodermia Osteodysplastica/Wrinkly Skin Syndrome: Report of Three Patients and Brief Review of the Literature. [JOURNAL ARTICLE]
Pediatr Dermatol 2008 Jan; 25(1):66-71.
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Tüysüz B, Arapoğlu M, Ilikkan B, et al. 
Congenital cutis laxa syndrome: type II autosomal recessive inheritance. [Case Reports, Journal Article]
Turk J Pediatr 2003 Jul-Sep; 45(3):265-8.
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Rajab A, Kornak U, Budde BS, et al. 
Geroderma osteodysplasticum hereditaria and wrinkly skin syndrome in 22 patients from Oman. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Mar 17.
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Imaizumi K, Kurosawa K, Makita Y, et al. 
Male with type II autosomal recessive cutis laxa. [Case Reports, Journal Article]
Clin Genet 1994 Jan; 45(1):40-3.
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Rybojad M, Baumann C, Godeau G, et al. 
[Congenital generalized cutis laxa: 5 cases] [Case Reports, Journal Article]
Ann Dermatol Venereol 1999 Apr; 126(4):317-9.
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Morava E, Lefeber DJ, Urban Z, et al. 
Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation. [JOURNAL ARTICLE]
Eur J Hum Genet 2007 Oct 31.
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Robertson SP, Bankier A 
Sotos syndrome and cutis laxa. [Case Reports, Journal Article]
J Med Genet 1999 Jan; 36(1):51-6.
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