Neonatal diagnosis of Kindler syndrome

This publication has 9 references indexed in Scilit:

• An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene
  Clinical and Experimental Dermatology, 2005
• Kindler Syndrome in Native Americans From Panama
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• Kindler syndrome
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• Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome
  Journal of Investigative Dermatology, 2004
• A Novel Nonsense Mutation in Kindler Syndrome
  Journal of Investigative Dermatology, 2004
• Loss of Kindlin-1, a Human Homolog of the Caenorhabditis elegans Actin–Extracellular-Matrix Linker Protein UNC-112, Causes Kindler Syndrome
  American Journal of Human Genetics, 2003
• Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome
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• Kindler syndrome complicated by squamous cell carcinoma of the hard palate: successful treatment with high-dose radiation therapy and granulocyte-macrophage colony-stimulating factor
  British Journal of Dermatology, 2001
• CONGENITAL POIKILODERMA WITH TRAUMATIC BULLA FOKMATION AND PROGRESSIVE CUTANEOUS ATROPHY.
  British Journal of Dermatology, 1954