| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 18348262 [Unique ID], provided by the PubMed system | |
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| | 1 - 10 of 101 journal articles in the PubMed database | Email to a friend | | |
| 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.
Abstract | Full Citation | Find Related Articles | | 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.
Abstract | Full Citation | Find Related Articles | | Al-Gazali LI, Sztriha L, Skaff F, et al.
Gerodermia osteodysplastica and wrinkly skin syndrome: are they the same? [Case Reports, Journal Article]
Am J Med Genet 2001 Jul 1; 101(3):213-20.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | 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.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | 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.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | 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.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | 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.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Kreuz FR, Wittwer BH
Del(2q)--cause of the wrinkly skin syndrome? [Case Reports, Journal Article, Review]
Clin Genet 1993 Mar; 43(3):132-8.
Abstract | Full Citation | Find Related Articles | | Kunze J, Majewski F, Montgomery P, et al.
De Barsy syndrome--an autosomal recessive, progeroid syndrome. [Journal Article]
Eur J Pediatr 1985 Nov; 144(4):348-54.
Abstract | Full Citation | Find Related Articles |   |
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