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Articles related to 17014644 [Unique ID], provided by the PubMed system
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Boente Mdel C, Asial RA, Winik BC 
Geroderma osteodysplastica. Report of a new family. [Journal Article]
Pediatr Dermatol 2006 Sep-Oct; 23(5):467-72.
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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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Hunter AG 
Is geroderma osteodysplastica underdiagnosed? [Case Reports, Journal Article]
J Med Genet 1988 Dec; 25(12):854-7.
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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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Hunter AG, Martsolf JT, Baker CG, et al. 
Geroderma osteodysplastica. A report of two affected families. [Journal Article]
Hum Genet 1978 Feb 16; 40(3):311-24.
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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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Tsukahara M, Shinkai H, Asagami C, et al. 
A disease with features of cutis laxa and Ehlers-Danlos syndrome. Report of a mother and daughter. [Case Reports, Journal Article]
Hum Genet 1988 Jan; 78(1):9-12.
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Boente MC, Winik BC, Asial RA 
Wrinkly skin syndrome: ultrastructural alterations of the elastic fibers. [Case Reports, Journal Article]
Pediatr Dermatol 1999 Mar-Apr; 16(2):113-7.
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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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