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Prenatal detection of Canavan disease by measurement ofN-acetyl-l-aspartate in amniotic fluid

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Journal of Inherited Metabolic Disease

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References

  • Jakobs C, ten-Brink HJ, Divry P, Rolland MO (1992) Prenatal diagnosis of Canavan disease (letter).Eur J Pediatr 151: 620.

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  • Kelley RI, Stamas JN (1991) Quantification ofN-acetyl-l-aspartic acid in urine by isotope-dilution gas chromatography/mass spectrometry.J Inher Metab Dis 15: 97–104.

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  • Matalon R, Michals K, Gashkoff P, Kaul R (1992) Prenatal diagnosis of Canavan disease.J Inher Metab Dis 15: 392–394.

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Authors and Affiliations

  1. Department of Pediatrics, Johns Hopkins University School of Medicine, 21205, Baltimore, MD, USA

    R. I. Kelley

  2. the Division of Neurogenetics, Kennedy Krieger Institute, 707 North Broadway, 21205, Baltimore, MD, USA

    R. I. Kelley

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  1. R. I. Kelley
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Kelley, R.I. Prenatal detection of Canavan disease by measurement ofN-acetyl-l-aspartate in amniotic fluid. J Inherit Metab Dis 16, 918–919 (1993). https://doi.org/10.1007/BF00714302

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  • DOI: https://doi.org/10.1007/BF00714302

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