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Heterozygous nonsense variants in the ferritin heavy-chain gene FTH1 cause a neuroferritinopathy
UploadDe novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome
Download from onlinelibrary.wiley.comPublisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders
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Download from onlinelibrary.wiley.comGenetics workforce: distribution of genetics services and challenges to health care in California
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