𝔖 Bobbio Scriptorium

✦ LIBER ✦

Newborn screening in fabry disease: What can be achieved with early diagnosis?

✍ Scribed by Olaf A. Bodamer

Book ID: 117321825
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 53 KB
Volume: 30
Category: Article
ISSN: 0149-2918
DOI: 10.1016/s0149-2918(08)80035-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

RUNX1 gene mutation in primary myelodysp

RUNX1 gene mutation in primary myelodysplastic syndrome – the mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome

✍ Chien-Yuan Chen; Liang-In Lin; Jih-Luh Tang; Bo-Sheng Ko; Woei Tsay; Wen-Chien C 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 306 KB