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1. Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.

2. Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa

4. Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis

8. Site-specific recombination in the cyanobacterium Anabaena sp. strain PCC 7120 catalyzed by the integrase of coliphage HK022

9. Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population

11. Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis

12. Epidermolytic Ichthyosis Sine Epidermolysis

13. SVEP1 plays a crucial role in epidermal differentiation

14. Loss-of-Function Mutations in SERPINB8 Linked to Exfoliative Ichthyosis with Impaired Mechanical Stability of Intercellular Adhesions

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