Genetics
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18 june 2018 20:03:27 |
| Utility of two SMN1 variants to improve spinal muscular atrophy carrier diagnosis and genetic counselling (European Journal of Human Genetics) |
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| 107 viewsCategory: Genetics |
 SET de novo frameshift variants associated with developmental delay and intellectual disabilities (European Journal of Human Genetics)Phenotypic spectrum of Au-Kline syndrome: a report of six new cases and review of the literature (European Journal of Human Genetics) 
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