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Clinical Genetics
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March 9, 2026
Deep-Intronic Variant in RUNX2 Causing Pseudo-Exon Inclusion in a Family With Cleidocranial Dysplasia
Dorothea Stojanovic, Dorota Garczarczyk-Asim, Julia Vodopiutz, et al.
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Search research articles
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Showing results (1-10 of 1) with videos related to
Sort By:
Page
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Clinical Genetics
|
March 9, 2026
Deep-Intronic Variant in RUNX2 Causing Pseudo-Exon Inclusion in a Family With Cleidocranial Dysplasia
Dorothea Stojanovic, Dorota Garczarczyk-Asim, Julia Vodopiutz, et al.
Page
of 1