Genetics
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5 december 2019 21:00:21 |
| A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder (European Journal of Human Genetics) |
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| 274 viewsCategory: Genetics |
 `Patient Journeys`: improving care by patient involvement (European Journal of Human Genetics)Primary care provider perspectives on using genomic sequencing in the care of healthy children (European Journal of Human Genetics) 
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