Mutations in Capillary Morphogenesis Gene-2 Result in the Allelic Disorders Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis

This publication has 29 references indexed in Scilit:

• The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21
  American Journal of Human Genetics, 2002
• A high-resolution recombination map of the human genome
  Nature Genetics, 2002
• Nonmuscle Myosin Heavy Chain IIA Mutations Define a Spectrum of Autosomal Dominant Macrothrombocytopenias: May-Hegglin Anomaly and Fechtner, Sebastian, Epstein, and Alport-Like Syndromes
  American Journal of Human Genetics, 2001
• Functional Interplay between Type I Collagen and Cell Surface Matrix Metalloproteinase Activity
  Journal of Biological Chemistry, 2001
• Two Siblings with Juvenile Hyaline Fibromatosis: Case Reports and Review of the Literature
  Clinical Rheumatology, 1999
• A homozygous mutation in the integrin alpha6 gene in junctional epidermolysis bullosa with pyloric atresia.
  Journal of Clinical Investigation, 1997
• Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia
  Nature Genetics, 1995
• Improved methods for building protein models in electron density maps and the location of errors in these models
  Acta Crystallographica Section A Foundations of Crystallography, 1991
• Juvenile hyaline fibromatosis: Two new patients and review of the literature
  American Journal of Medical Genetics, 1987
• Infantile Systemic Hyalinosis: Report of Four Cases of a Disease, Fatal in Infancy, Apparently Different from Juvenile Systemic Hyalinosis
  Pediatric Pathology, 1986