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| Genomic newborn screening: BabyScreen+ v0.1386 | SLX4 |
Zornitza Stark Tag treatable tag was added to gene: SLX4. Tag haematological tag was added to gene: SLX4. |
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| Genomic newborn screening: BabyScreen+ v0.1364 | SLX4 | Seb Lunke Marked gene: SLX4 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.1364 | SLX4 | Seb Lunke Gene: slx4 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.1364 | SLX4 | Seb Lunke reviewed gene: SLX4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fanconi anaemia, complementation group P, MIM# 613951; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | SLX4 |
Zornitza Stark gene: SLX4 was added gene: SLX4 was added to gNBS. Sources: BeginNGS,Expert Review Green Mode of inheritance for gene: SLX4 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SLX4 were set to Fanconi anaemia, complementation group P, MIM# 613951 |
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