Activity
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Monogenic hearing loss v2.239
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GRHL2
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Arina Puzriakova Phenotypes for gene: GRHL2 were changed from hearing loss; Deafness, autosomal dominant 28, 608641; #616029: Ectodermal dysplasia/short stature syndrome to Deafness, autosomal dominant 28, OMIM:608641; Ectodermal dysplasia/short stature syndrome, OMIM:616029
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Monogenic hearing loss v1.43
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GRHL2
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Ellen McDonagh commented on gene: GRHL2: New review confirms gene status and mode of inheritance; no changes required.
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Monogenic hearing loss
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GRHL2
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Lampros Mavrogiannis reviewed GRHL2
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