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| BabyScreen+ newborn screening v0.2148 | CRYM | Zornitza Stark Marked gene: CRYM as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.2148 | CRYM | Zornitza Stark Gene: crym has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.2148 | CRYM | Zornitza Stark Classified gene: CRYM as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.2148 | CRYM | Zornitza Stark Gene: crym has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.2141 | CRYM |
Lilian Downie gene: CRYM was added gene: CRYM was added to Baby Screen+ newborn screening. Sources: Expert list Mode of inheritance for gene: CRYM was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: CRYM were set to PMID: 12471561, 32742378 Phenotypes for gene: CRYM were set to Deafness, autosomal dominant 40 MIM#616357 Review for gene: CRYM was set to RED Added comment: Dominant hearing loss One paper infant onset, the other all adult onset Sources: Expert list |
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