共 50 条
- [3] A novel deletion mutation in IL2RG gene results in X-linked severe combined immunodeficiency with an atypical phenotype Immunogenetics, 2017, 69 : 29 - 38
- [8] Diversity in Phenotype of Two Siblings and their with X-Linked Hypophosphatemic Rickets due to PHEX Mutation HORMONE RESEARCH IN PAEDIATRICS, 2016, 86 : 189 - 189