X-linked anhidrotic ectodermal dysplasia and de novo t(X;1) in a female

This publication has 14 references indexed in Scilit:

• Female with hypohidrotic ectodermal dysplasia and de novo (X;9) translocation
  Human Genetics, 1990
• X‐linked hypohidrotic ectodermal dysplasia and t(X;12) in a female
  Clinical Genetics, 1989
• Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker
  Human Genetics, 1988
• Clinical aspects of X-linked hypohidrotic ectodermal dysplasia.
  Archives of Disease in Childhood, 1987
• X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization
  Human Genetics, 1987
• Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12
  Human Genetics, 1986
• Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome)
  Human Genetics, 1986
• Expression of X‐linked hypohidrotic ectodermal dysplasia in six males and in their mothers
  Clinical Genetics, 1985
• X-Autosome translocations: Cytogenetic characteristics and their consequences
  Human Genetics, 1982
• Two human X-autosome translocations identified by autoradiography and fluorescence.
  1972