Associated Papers
A Novel Heterozygous IHH c.331_333del Mutation Identified in a Fetus with Brachydactyly Type A1 Causes IHH Protein Maturation Failure in HEK293T Cells.
Zhu T et al.
Phenomics (cham, Switzerland), 2025
Whole-exome sequencing identifies a novel IHH insertion in an Ontario family with brachydactyly type A1.
Ho R et al.
Sage Open Medical Case Reports, 2018
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