Case Report: Cervical Lipoblastoma in a Child with a KCTD7 Mutation. Heterozygous Variants in LRP1 Cause a Distinct Neurodevelopmental Disorder with Congenital Heart Disease
Product Description:
Genetic Medicine
Product/Publication Type(s):
Peer-reviewed publications in scholarly journals submitted
Target Audience:
Professionals, Policymakers, Students
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