دورية أكاديمية
O10 Universal genomic newborn screening for early, treatable, and severe conditions- including 33 genes of NMD: Baby Detect
| العنوان: | O10 Universal genomic newborn screening for early, treatable, and severe conditions- including 33 genes of NMD: Baby Detect |
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| المؤلفون: | Dangouloff, T., Hovhannesyan, K., Piazzon, F., Mashhadizadeh, D., Helou, L., Palmeira, L., Boemer, F., Servais, L. |
| المصدر: | In Neuromuscular Disorders October 2023 33 Supplement 1:S130-S131 |
| قاعدة البيانات: | ScienceDirect |
Full Text via ClinicalKey 
Full Text Finder | تدمد: | 09608966 |
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| DOI: | 10.1016/j.nmd.2023.07.259 |