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Studies on a case of persistent hyperlysinaemia with a possible method for prenatal diagnosis

1983; Springer Science+Business Media; Volume: 6; Issue: S2 Linguagem: Inglês

10.1007/bf01810354

1573-2665

R. G. F. Gray, M. J. Bennett, A. Green, N. A. Boyle, J G Feeney, P. Jackson, R. J. Pollitt,

Neonatal Health and Biochemistry

Journal of Inherited Metabolic DiseaseVolume 6, Issue S2 p. 115-116 Short Communication Studies on a case of persistent hyperlysinaemia with a possible method for prenatal diagnosis R. G. F. Gray, R. G. F. Gray Sub-Department of Medical Genetics, University of Sheffield, Sheffield, S10 5DN UKSearch for more papers by this authorM. J. Bennett, M. J. Bennett Department of Chemical Pathology, Sheffield Children's Hospital, Sheffield, S10 2TN UKSearch for more papers by this authorA. Green, A. Green Department of Chemical Pathology, Sheffield Children's Hospital, Sheffield, S10 2TN UKSearch for more papers by this authorN. A. Boyle, N. A. Boyle Departments of Paediatrics, Obstetrics and Biochemistry, Huddersfield Royal Infirmary, Huddersfield, UKSearch for more papers by this authorJ. G. Feeney, J. G. Feeney Departments of Paediatrics, Obstetrics and Biochemistry, Huddersfield Royal Infirmary, Huddersfield, UKSearch for more papers by this authorP. Jackson, P. Jackson Departments of Paediatrics, Obstetrics and Biochemistry, Huddersfield Royal Infirmary, Huddersfield, UKSearch for more papers by this authorR. J. Pollitt, R. J. Pollitt Neonatal Screening Laboratory, Middlewood Hospital, Sheffield, S6 1TP UKSearch for more papers by this author R. G. F. Gray, R. G. F. Gray Sub-Department of Medical Genetics, University of Sheffield, Sheffield, S10 5DN UKSearch for more papers by this authorM. J. Bennett, M. J. Bennett Department of Chemical Pathology, Sheffield Children's Hospital, Sheffield, S10 2TN UKSearch for more papers by this authorA. Green, A. Green Department of Chemical Pathology, Sheffield Children's Hospital, Sheffield, S10 2TN UKSearch for more papers by this authorN. A. Boyle, N. A. Boyle Departments of Paediatrics, Obstetrics and Biochemistry, Huddersfield Royal Infirmary, Huddersfield, UKSearch for more papers by this authorJ. G. Feeney, J. G. Feeney Departments of Paediatrics, Obstetrics and Biochemistry, Huddersfield Royal Infirmary, Huddersfield, UKSearch for more papers by this authorP. Jackson, P. Jackson Departments of Paediatrics, Obstetrics and Biochemistry, Huddersfield Royal Infirmary, Huddersfield, UKSearch for more papers by this authorR. J. Pollitt, R. J. Pollitt Neonatal Screening Laboratory, Middlewood Hospital, Sheffield, S6 1TP UKSearch for more papers by this author First published: 01 June 1983 https://doi.org/10.1007/BF01810354Citations: 3AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1Dancis J., Hutzler J., Cox P. R. (1979) Familial hyperlysinemia; enzyme studies, diagnostic methods, comments on terminology. Am. J. Hum. Genet., 31: 290–299. CASPubMedWeb of Science®Google Scholar 2Rosenberg L. E., Scriver C. R., Bondy P. K., Rosenberg L. E. (1980) Disorders of amino acid metabolism. In: Metabolic Control and Disease, Philadelphia: Saunders, 678–681. Google Scholar Citing Literature Volume6, IssueS2June 1983Pages 115-116 ReferencesRelatedInformation