True hermaphroditism with partial duplication of chromosome 22 and withoutSRY

This publication has 16 references indexed in Scilit:

• A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome.
  Journal of Medical Genetics, 1995
• Trisomy 22 and intersex.
  Archives of Disease in Childhood: Fetal & Neonatal, 1994
• The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism
  Human Genetics, 1992
• Use of probes for ZFY, SRY, and the Y pseudoautosomal boundary in XX males, XX true hermaphrodites, and an XY female.
  Journal of Medical Genetics, 1991
• A ZFY-negative 46,XX true hermaphrodite is positive for the Y pseudoautosomal boundary
  Human Genetics, 1990
• Familial XX chromosomal maleness does not arise from a Y chromosomal translocation
  The Journal of Pediatrics, 1989
• Familial XX true hermaphroditism and the H-Y antigen
  Human Genetics, 1979
• Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy.
  Journal of Medical Genetics, 1977
• AN XX/XY HUMAN HERMAPHRODITE RESULTING FROM DOUBLE FERTILIZATION
  Proceedings of the National Academy of Sciences, 1962
• True Hermaphrodite Siblings
  Journal of Urology, 1958