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. 1993 Sep;69(815):669–671. doi: 10.1136/pgmj.69.815.669

Who should be offered genetic screening?

PMCID: PMC2399775 PMID: 8255830

669

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Pergolizzi R. G., Erster S. H., Goonewardena P., Brown W. T. Detection of full fragile X mutation. Lancet. 1992 Feb 1;339(8788):271–272. doi: 10.1016/0140-6736(92)91334-5. [DOI] [PubMed] [Google Scholar]
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