Found: 7
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Implementation of the newborn screening programme for sickle cell disease in England: results for 2003–2005.
- Published in:
- Journal of Medical Screening, 2008, v. 15, n. 1, p. 9, doi. 10.1258/jms.2008.007063
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- Publication type:
- Article
Bohring-Opitz (Oberklaid-Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 5, p. 513, doi. 10.1038/ejhg.2010.234
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- Publication type:
- Article
Cross-sectional audit assessing the quality of dried bloodspot specimens received by UK metabolic biochemistry laboratories for the biochemical monitoring of individuals with Phenylketonuria.
- Published in:
- Annals of Clinical Biochemistry, 2023, v. 60, n. 3, p. 208, doi. 10.1177/00045632231156035
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- Publication type:
- Article
Point of care testing: making innovation work for patient-centred care.
- Published in:
- 2013
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- Publication type:
- journal article
Isolation of human genomic DNA for genetic analysis from premature neonates: a comparison between newborn dried blood spots, whole blood and umbilical cord tissue.
- Published in:
- BMC Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2156-14-105
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- Publication type:
- Article
Isolated aortic root dilation in homocystinuria.
- Published in:
- Journal of Inherited Metabolic Disease, 2018, v. 41, n. 1, p. 109, doi. 10.1007/s10545-017-0094-7
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- Publication type:
- Article
Incidental Detection of Classical Galactosemia through Newborn Screening for Phenylketonuria: A 10-Year Retrospective Audit to Determine the Efficacy of This Approach.
- Published in:
- International Journal of Neonatal Screening (IJNS), 2024, v. 10, n. 1, p. 2, doi. 10.3390/ijns10010002
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- Publication type:
- Article