| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 14696810 [Unique ID], provided by the PubMed system | |
| |
|
| | 1 - 10 of 421 journal articles in the PubMed database | Email to a friend | | |
| 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.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | de Schepper S, Loeys B, de Paepe A, et al.
Cutis laxa of the autosomal recessive type in a consanguineous family. [Case Reports, Journal Article]
Eur J Dermatol 2003 Nov-Dec; 13(6):529-33.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | 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.
Abstract | Full Citation | Find Related Articles | | 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.
Abstract | Full Citation | 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 | | Sarkar R, Kaur C, Kanwar AJ, et al.
Cutis laxa in seven members of a north-Indian family. [Journal Article]
Pediatr Dermatol 2002 May-Jun; 19(3):229-31.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Kermane A, Tachfouti S, Lezrek M, et al.
[Cutis laxa syndrome. Case report] [Case Reports, Journal Article]
Bull Soc Belge Ophtalmol 2004; (292):5-8.
Abstract | Full Citation | Find Related Articles | | Andiran N, Sarikayalar F, Saraçlar M, et al.
Autosomal recessive form of congenital cutis laxa: more than the clinical appearance. [Case Reports, Journal Article]
Pediatr Dermatol 2002 Sep-Oct; 19(5):412-4.
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 |   |
|
| |
Advertise on this site.
|
New! 