All individuals with variants in gene PRPH

1 entry on 1 page. Showing entry 1.
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00108467 28722276-FamPatIII3 PubMed: Hendee 2017, Journal: Hendee 2017 3-generation family, 10 affecteds (6F, 4M), PatIII3 M - United States Caucasian - 0 - - ? Congenital glaucoma Axenfeld-Rieger anomaly myopia sensorineural hearing loss congenital hypothyroidism arterial tortuosity microcephaly delayed eruption of permanent teeth femoral retroversion 1 1 Elena Semina
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