Development and physical analysis of YAC contigs covering 7 Mb of Xp22.3–p22.2

This publication has 37 references indexed in Scilit:

• A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata
  Human Molecular Genetics, 1993
• A Yeast Artificial Chromosome Contig Linking the Steroid Sulfatase and Kallmann Syndrome Loci on the Human X Chromosome Short Arm
  Genomics, 1993
• The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions
  Human Molecular Genetics, 1993
• Genetic Mapping of X-Linked Ocular Albinism: Linkage Analysis in a Large Newfoundland Kindred
  Genomics, 1993
• Isolation of a new gene from the distal short arm of the human X chromosome that escapes X-inactivation
  Human Molecular Genetics, 1992
• Linkage analysis in X-linked ocular albinism
  Genomics, 1991
• Testis cancer. Ichthyosis constitutes a significant risk factor
  Cancer, 1991
• Physical mapping of deletion breakpoints in patients with X-linked ichthyosis: evidence for clustering of distal and proximal breakpoints
  Proceedings Of The Royal Society B-Biological Sciences, 1990
• Long-range physical mapping around the human steroid sulfatase locus
  Genomics, 1990
• Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase
  Biochemical and Biophysical Research Communications, 1987