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- Ainsworth P. J., Surh L. C., Coulter-Mackie M. B. Diagnostic single strand conformational polymorphism, (SSCP): a simplified non-radioisotopic method as applied to a Tay-Sachs B1 variant. Nucleic Acids Res. 1991 Jan 25;19(2):405–406. doi: 10.1093/nar/19.2.405. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dworniczak B., Aulehla-Scholz C., Horst J. Phenylalanine hydroxylase gene: silent mutation uncovers evolutionary origin of different alleles. Clin Genet. 1990 Oct;38(4):270–273. doi: 10.1111/j.1399-0004.1990.tb03580.x. [DOI] [PubMed] [Google Scholar]
- Dworniczak B., Aulehla-Scholz C., Horst J. Phenylketonuria: detection of a frequent haplotype 4 allele mutation. Hum Genet. 1989 Dec;84(1):95–96. doi: 10.1007/BF00210683. [DOI] [PubMed] [Google Scholar]
- Dworniczak B., Grudda K., Stümper J., Bartholomé K., Aulehla-Scholz C., Horst J. Phenylalanine hydroxylase gene: novel missense mutation in exon 7 causing severe phenylketonuria. Genomics. 1991 Jan;9(1):193–199. doi: 10.1016/0888-7543(91)90238-a. [DOI] [PubMed] [Google Scholar]
- Orita M., Suzuki Y., Sekiya T., Hayashi K. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics. 1989 Nov;5(4):874–879. doi: 10.1016/0888-7543(89)90129-8. [DOI] [PubMed] [Google Scholar]