Alopecia areata universalis in an infant
Author:
Publisher
SAGE Publications
Subject
Dermatology,Surgery
Link
http://journals.sagepub.com/doi/pdf/10.1007/BF02737867
Reference31 articles.
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2. Lamartine J, Laoudj D, Blanchet-Bardon C, et al. Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French family. Br J Dermatol 2000; 142(2):248–252.
3. Kibar Z, Dube MP, Powell J, et al. Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping. Eur J Hum Genet 2000; 8(5):372–380.
4. Kibar Z, Lafreniere RG, Chakravarti A, et al. A radiation hybrid map of 48 loci including the Clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13q. Genomics 1999; 56(1):127–130.
5. Barth JH. Normal hair growth in children. Pediatr Dermatol 1987; 4(3):173–184.
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2. Onychomadesis: literature review;British Journal of Dermatology;2015-01-28
3. Selected topics in pediatric hair loss;Expert Review of Dermatology;2007-12
4. Infant alopecia universalis: role of topical PUVA (psoralen ultraviolet A) radiation;International Journal of Dermatology;2005-12
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