Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populations

This publication has 30 references indexed in Scilit:

• Progress in epidermolysis bullosa: from eponyms to molecular genetic classification
  Clinics in Dermatology, 2005
• Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2
  Human Molecular Genetics, 2003
• A Comparative Study of Immunohistochemistry and Electron Microscopy Used in the Diagnosis of Epidermolysis Bullosa
  The American Journal of Dermatopathology, 2003
• The clinical spectrum of nonbullous congenital ichthyosiform erythroderma and lamellar ichthyosis
  Clinical and Experimental Dermatology, 2003
• The molecular genetics of the genodermatoses: progress to date and future directions
  British Journal of Dermatology, 2003
• Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1
  Human Molecular Genetics, 2002
• Structural organization of cornified cell envelopes and alterations in inherited skin disorders
  Experimental Dermatology, 1998
• Transglutaminase 1 Mutations in Autosomal Recessive Congenital Ichthyosis: Private and Recurrent Mutations in an Isolated Population
  American Journal of Human Genetics, 1997
• Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosis
  Nature Genetics, 1995
• Heterogeneity in Autosomal Recessive Ichthyosis
  Archives of Dermatology, 1985