The gene for X-linked kallmann syndrome: a human neuronal migration defect

This publication has 30 references indexed in Scilit:

• Intragenic Deletion of theKALIG-1Gene in Kallmann's Syndrome
  New England Journal of Medicine, 1992
• A deletion map of the human Yq11 region: Implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis
  Genomics, 1991
• The WDNM1 gene product is a novel member of the ‘four-disulphide core’ family of proteins
  Biochemical and Biophysical Research Communications, 1991
• The cell adhesion molecule Cell‐CAM 105 is an ecto‐ATPase and a member of the immunoglobulin superfamily
  FEBS Letters, 1990
• Long-range physical mapping around the human steroid sulfatase locus
  Genomics, 1990
• Origin of luteinizing hormone-releasing hormone neurons
  Nature, 1989
• Contiguous gene syndromes: A component of recognizable syndromes
  The Journal of Pediatrics, 1986
• A new syndrome of anosmia, ichthyosis, hypogonadism, and various neurological manifestations with deficiency of steroid sulfatase and arylsulfatase C
  Annals of Neurology, 1986
• Heterogeneity of Kallmann's syndrome
  Clinical Genetics, 1985
• Familial Kallmann syndrome with unilateral renal aplasia
  Clinical Genetics, 1975