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Congenital adrenal hyperplasia cases identified by newborn screening in one- and two-screen states
There is no clear consensus among state newborn screening programs on whether routine second screening of newborns identifies clinically relevant cases of congenital adrenal hyperplasia. This retrospective study evaluated laboratory practices, along with biochemical and medical characteristics of co...
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| Foilsithe in: | Mol Genet Metab |
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| Main Authors: | , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4640991/ https://ncbi.nlm.nih.gov/pubmed/26296712 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2015.08.004 |
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