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
Deletion of 2 amino acids in IHH in a Japanese family with brachydactyly type A1.
Ozaki N et al.
Bmc Medical Genomics, 2021
Severe Form of Brachydactyly Type A1 in a Child with a c.298G > A Mutation in IHH Gene.
Salian S et al.
Journal of Pediatric Genetics, 2017
Reprint of: Heparan sulfate as a regulator of endochondral ossification and osteochondroma development.
Jochmann K et al.
Matrix Biology : Journal of the International Society for Matrix Biology, 2014
Heparan sulfate as a regulator of endochondral ossification and osteochondroma development.
Jochmann K et al.
Matrix Biology : Journal of the International Society for Matrix Biology, 2014
Brachydactyly type A1 associated with unusual radiological findings and a novel Arg158Cys mutation in the Indian hedgehog (IHH) gene.
Stattin EL et al.
European Journal of Medical Genetics, 0
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