ReviewGenes2021
The Diagnostic Journey of a Patient with Prader-Willi-Like Syndrome and a Unique Homozygous
Karlijn Pellikaan et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
4 papers cite it
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ReviewGenes2021
Karlijn Pellikaan et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.