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. 1990 Jan;27(1):65–66. doi: 10.1136/jmg.27.1.65

Application of a new DNA sequence polymorphism as a genetic marker in prenatal diagnosis of phenylketonuria.

S Z Huang ¹, Z R Ren ¹, Y T Zeng ¹

PMCID: PMC1016886 PMID: 1968515

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Selected References

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

DiLella A. G., Huang W. M., Woo S. L. Screening for phenylketonuria mutations by DNA amplification with the polymerase chain reaction. Lancet. 1988 Mar 5;1(8584):497–499. doi: 10.1016/s0140-6736(88)91295-0. [DOI] [PubMed] [Google Scholar]
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