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2011 | 1 |
2015 | 1 |
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Single newborn screen or routine second screening for primary congenital hypothyroidism.
Mol Genet Metab. 2015 Nov;116(3):125-32. doi: 10.1016/j.ymgme.2015.08.003. Epub 2015 Aug 11.
Mol Genet Metab. 2015.
PMID: 26293295
Free PMC article.
Lysosomal storage diseases: diagnostic confirmation and management of presymptomatic individuals.
Wang RY, Bodamer OA, Watson MS, Wilcox WR; ACMG Work Group on Diagnostic Confirmation of Lysosomal Storage Diseases.
Wang RY, et al.
Genet Med. 2011 May;13(5):457-84. doi: 10.1097/GIM.0b013e318211a7e1.
Genet Med. 2011.
PMID: 21502868
Free article.
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