Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: Implication for the MRX locus

This publication has 28 references indexed in Scilit:

• An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3–Xp21.3
  Human Molecular Genetics, 1995
• Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome
  Nature Genetics, 1995
• A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy
  Cell, 1995
• Development and physical analysis of YAC contigs covering 7 Mb of Xp22.3–p22.2
  Genomics, 1995
• A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
  Nature, 1991
• Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.
  Proceedings of the National Academy of Sciences, 1989
• Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis.
  Proceedings of the National Academy of Sciences, 1987
• Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis.
  Proceedings of the National Academy of Sciences, 1987
• Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase
  Biochemical and Biophysical Research Communications, 1987
• Interrelation of the therapeutic effects of growth hormone and testosterone on growth in hypopituitarism
  The Journal of Pediatrics, 1976