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Keratosis pilaris and ulerythema ophryogenes in a woman with monosomy of the short arm of chromosome 18. [Case Reports, Journal Article]
An Bras Dermatol 2011 Jul-Aug; 86(4 Suppl 1):S42-5.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Siegel DH, Mann JA, Krol AL, et al.
Dermatological phenotype in Costello syndrome: consequences of Ras dysregulation in development. [Journal Article, Research Support, N.I.H., Extramural]
Br J Dermatol 2012 Mar; 166(3):601-7.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Dianzani C, Pizzuti A, Gaspardini F, et al.
Ulerythema ophryogenes, a rare and often misdiagnosed syndrome: analysis of an idiopathic case. [Case Reports, Letter]
Int J Immunopathol Pharmacol 2011 Apr-Jun; 24(2):523-7.
Abstract | Full Citation | Find Related Articles | | Siegel DH, McKenzie J, Frieden IJ, et al.
Dermatological findings in 61 mutation-positive individuals with cardiofaciocutaneous syndrome. [Journal Article, Research Support, N.I.H., Extramural]
Br J Dermatol 2011 Mar; 164(3):521-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Castori M, Valiante M, Ritelli M, et al.
Palmoplantar keratoderma, pseudo-ainhum, and universal atrichia: A new patient and review of the palmoplantar keratoderma-congenital alopecia syndrome. [Case Reports, Journal Article, Review]
Am J Med Genet A 2010 Aug; 152A(8):2043-7.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Arnold AW, Buechner SA
[Keratosis pilaris and keratosis pilaris atrophicans faciei]. [Case Reports, English Abstract, Journal Article, Review]
J Dtsch Dermatol Ges 2006 Apr; 4(4):319-23.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Chien AJ, Valentine MC, Sybert VP
Hereditary woolly hair and keratosis pilaris. [Case Reports, Journal Article, Research Support, Non-U.S. Gov't]
J Am Acad Dermatol 2006 Feb; 54(2 Suppl):S35-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Klein OD, Cotter PD, Schmidt AM, et al.
Interstitial deletion of chromosome 12q: genotype-phenotype correlation of two patients utilizing array comparative genomic hybridization. [Case Reports, Journal Article]
Am J Med Genet A 2005 Nov 1; 138(4):349-54.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Manci EA, Martinez JE, Horenstein MG, et al.
Cardiofaciocutaneous syndrome (CFC) with congenital peripheral neuropathy and nonorganic malnutrition: an autopsy study. [Case Reports, Journal Article]
Am J Med Genet A 2005 Aug 15; 137(1):1-8.
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