Haaranomalien bei syndromalen Erkrankungen
Author:
Publisher
Springer Science and Business Media LLC
Subject
Dermatology
Link
http://link.springer.com/content/pdf/10.1007/s00105-019-4440-6.pdf
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3. Betz RC, Cabral RM, Christiano AM, Sprecher E (2012) Unveiling the roots of monogenic genodermatoses: genotrichoses as a paradigm. J Invest Dermatol 132:906–914
4. Vergano SS, Deardorff MA (2014) Clinical features, diagnostic criteria, and management of Coffin-Siris syndrome. Am J Med Genet C Semin Med Genet 166C:252–256
5. Price VH, Odom RB, Ward WH, Jones FT (1980) Trichothiodystrophy: sulfur-deficient brittle hair as a marker for a neuroectodermal symptom complex. Arch Dermatol 116:1375–1384
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