Fragile X syndrome: Diagnostic and carrier testing

@inproceedings{Sherman2005FragileXS,
  title={Fragile X syndrome: Diagnostic and carrier testing},
  author={Stephanie G Sherman and Beth A. Pletcher and Deborah Anne Driscoll},
  booktitle={Genetics in Medicine},
  year={2005}
}
Disclaimer: This guideline is designed primarily as an educational resource for medical geneticists and other health care providers to help them provide quality medical genetic services. Adherence to this guideline does not necessarily assure a successful medical outcome. This guideline should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results. In determining the propriety of any… CONTINUE READING

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Striking neurological symptoms in normal transmitting males of the fragile X syndrome

  • A Smits, W van der Bruggen, E Sistermans, B Kiemeney, W Reneir, B. Kremer
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