| Hanemann JA, de Carvalho BC, Franco EC
Oral manifestations in Ellis-van Creveld syndrome: report of a case and review of the literature. [Case Reports, Journal Article, Review]
J Oral Maxillofac Surg 2010 Feb; 68(2):456-60.
Full Citation | Publisher Full Text | Find Related Articles | | Mihçi E, Erişir S, Taçoy S, et al.
Aplasia cutis congenita: three cases with three different underlying etiologies. [Journal Article]
Turk J Pediatr 2009 Sep-Oct; 51(5):510-4.
Abstract | Full Citation | | Al Balwi M, Ibrahim AA, Abdulrahman AS
Novel human pathological mutations. Gene symbol: EDAR. Disease: Ectodermal dysplasia, hypohidrotic. [Journal Article]
Hum Genet 2010 Jan; 127(1):123.
Full Citation | Find Related Articles | | Ebtisam E
Hereditary palmoplantar keratoderma: A rare case report--pachyonychia congenita (PC). [Case Reports, Journal Article]
Dermatol Nurs 2009 Nov-Dec; 21(6):351-3.
Full Citation | Find Related Articles | | Kohli N
Pachyonychia congenita: a case report. [Journal Article]
Cutis 2009 Nov; 84(5):269-71.
Abstract | Full Citation | | Lexner MO, Almer L
Case series: Treatment considerations in x-linked hypohidrotic ectodermal dysplasia. [Journal Article]
Eur Arch Paediatr Dent 2009 Nov.:26-30.
Abstract | Full Citation | Find Related Articles | | Bowden PE
Mutations in a Keratin 6 Isomer (K6c) Cause a Type of Focal Palmoplantar Keratoderma. [JOURNAL ARTICLE]
J Invest Dermatol 2010 Feb; 130(2):336-338.
Abstract | Full Citation | | Proceedings of the International Research Symposium on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) Syndrome, November 8-10, 2006, Houston, Texas, USA. [Congresses, Overall]
Am J Med Genet A 2009 Sep; 149A(9):1885-957.
Full Citation | | Schnabl SM, Horch RE, Ganslandt O, et al.
Aplasia Cutis Congenita - Plastic Reconstruction of three Scalp and Skull Defects with two Opposed Scalp Rotation Flaps and Split Thickness Skin Grafting. [JOURNAL ARTICLE]
Neuropediatrics 2009 Aug; 40(3):134-136.
Abstract | Full Citation | | McCarl CA, Picard C, Khalil S, et al.
ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
J Allergy Clin Immunol 2009 Dec; 124(6):1311-1318.e7.
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