Browsing by Author "Allen, C.L."
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- ItemHIST1H1E heterozygous protein-truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt : A study to clarify the HIST1H1E syndrome phenotype in 30 individuals(2019) Burkardt, D.D.; Zachariou, A.; Loveday, C.; Allen, C.L.; Amor, D.J.; Ardissone, A.; Banka, S.; Bourgois, A.; Coubes, C.; Lay-Son Rodríguez, Guillermo Roberto