Genetic Hair Disorders

Author:

Durán-McKinster Carola

Publisher

Springer New York

Reference63 articles.

1. Shao L, Newell B. Light microscopic hair abnormalities in children: retrospective review of 119 cases in a 10-year period. Pediatr Dev Pathol. 2014;17(1):36–43 [Epub ahead of print].

2. Celep F, Uzumcu A, Sonmez FM, et al. Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance. Genet Couns. 2009;20:1–8.

3. Singh G, Siddalingappa K, Nischal KC, Chandra Naik L, Lokanatha K. Monilethrix in three generations. Indian J Dermatol. 2008;53:99–100.

4. Ye ZZ, Nan X, Zhao HS, et al. Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital Monilethrix. Chin Med J (Engl). 2013;126(16):3103–6.

5. De Cruz R, Horev L, Green J, et al. A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance. Br J Dermatol. 2012;166 Suppl 2:20–6.

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