Associated Papers
Prevalence of monogenic disease in paediatric patients with a predominant respiratory phenotype.
Dai D et al.
Archives of Disease in Childhood, 2022
34134972 (PubMed )
Supplement: archdischild-2021-322058supp001.pdf
The clinical, immunological and genetic features of 12 Chinese patients with STAT3 mutations.
Lin L et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology, 2020
[Clinical features and molecular diagnosis of three patients with DiGeorge anomaly].
Sun JQ et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2012
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