ArticleAnnals of human genetics2022
A splice site variant in TCTN3 underlies an atypical form of orofaciodigital syndrome IV.
Shabir Hussain et al.PubMed ↗Full text ↗Publisher ↗
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ArticleAnnals of human genetics2022
Shabir Hussain et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.