Neonatal screening for hereditary tyrosinaemia: are we there yet?

Hadzic, Nedim; Vara, Roshni

doi:10.1136/archdischild-2015-308265

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Neonatal screening for hereditary tyrosinaemia: are we there yet?

Author(s): Nedim Hadžić ¹ , Roshni Vara ²

Publication date (Electronic): Aug 2015

Journal: Archives of disease in childhood

Publisher: BMJ

Keywords: Hepatology, Metabolic, Paediatric Practice

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Journal ID (iso-abbrev): Arch Dis Child

Title: Archives of disease in childhood

Publisher: BMJ

ISSN (Electronic): 1468-2044

ISSN (Print): 0003-9888

Publication date (Electronic): Aug 2015

Volume: 100

Issue: 8

Affiliations

[1 ] Paediatric Centre for Hepatology, Gastroenterology and Nutrition, King's College Hospital, London, UK.

[2 ] Metabolic Medicine, Evelina Children's Hospital, London, UK.

Article

Publisher Item ID: archdischild-2015-308265

DOI: 10.1136/archdischild-2015-308265

PubMed ID: 25957320

SO-VID: 6b64dc7e-26fc-4e69-9571-fee5910d6c9e

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Keywords: Metabolic,Hepatology,Paediatric Practice

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Keywords: Metabolic, Hepatology, Paediatric Practice

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Neonatal screening for hereditary tyrosinaemia: are we there yet?

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Pediatric Pulse: Advancing Neonatal and Child Health

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