Phenylketonuria in the Netherlands%2525253A 93%25252525 of t…
Phenylketonuria in the Netherlands%2525253A 93%25252525 of the mutations are detected by single-strand conformation analysis.
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Journal:
Human HeredityOpens in new Window
Collection:
Karger UKB (inactive subscribed)
Coverage:
- 1998~2021
Journal:
Human HeredityOpens in new Window
Collection:
Karger Open Access Journals
Coverage:
- 2022-01-01~present
Journal:
Human HeredityOpens in new Window
Collection:
Karger (voormalige SurfMarket deal) Nijmegen
Coverage:
- 1998~2015