Fragile X transmission and the determination of carrier probabilities for genetic counselling

This publication has 12 references indexed in Scilit:

• Phenotypic variation in male‐transmitted fragile X: Genetic inferences
  American Journal of Medical Genetics, 1987
• Prenatal diagnosis of the fragile X using thymidine induction
  Prenatal Diagnosis, 1987
• Autosomal suppressor gene for fragile‐X: An hypothesis
  American Journal of Medical Genetics, 1987
• Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome
  Human Genetics, 1986
• Inheritance of fragile X syndrome: An hypothesis
  American Journal of Medical Genetics, 1986
• Speculation on the role of transposable elements in human genetic disease with particular attention to achondroplasia and the fragile X syndrome
  American Journal of Medical Genetics, 1986
• Second international workshop on the fragile X and on X‐linked mental retardation
  American Journal of Medical Genetics, 1986
• A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation
  American Journal of Medical Genetics, 1985
• Further segregation analysis of the fragile X syndrome with special reference to transmitting males
  Human Genetics, 1985
• The marker (X) syndrome: a cytogenetic and genetic analysis
  Annals of Human Genetics, 1984