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Paper Details

The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.
Human Molecular Genetics
62
1997
22q11, CATCH22, DiGeorge, DiGeorge syndrome, HIRA, Hir2p, Hira, Hira expressing cell populations, alternatively spliced transcripts, birth defects, chromatin, cranio-facial, cardiac and thymic malformations, haploinsufficiency of HIRA, hindbrain neural crest cells, histone, human, human Chromatin Assembly Factor I, mammalian embryos, mouse, murine, murine embryonic cDNAs, p60 subunit, patients, transcripts, yeast, yeast hir1p
Author NameAffiliation
Laurens G WilmingInstitute of Pediatric Surgery, Erasmus University
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