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1.
Analysis of gene variation and long-term follow-up in children with phenylalanine hydroxylase deficiency diagnosed by newborn screening / 浙江大学学报·医学版
Journal of Zhejiang University. Medical sciences
; (6): 701-706, 2023.
Artículo
en Inglés
| WPRIM | ID: wpr-1009945
2.
Analysis of biochemical and genetic screening results for neonatal methylmalonic acidemia / 中华实用儿科临床杂志
Chinese Journal of Applied Clinical Pediatrics
; (24): 54-59, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-989990
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