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Publications by Wenjuan Qiu
Mutational Spectrum of Phenylketonuria in the Chinese Han Population: A Novel Insight Into the Geographic Distribution of the Common Mutations
Pediatric Research
Child Health
Pediatrics
Perinatology
Uniparental Isodisomy Caused Autosomal Recessive Diseases: NGS‐based Analysis Allows the Concurrent Detection of Homogenous Variants and Copy‐neutral Loss of Heterozygosity
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Novel PYGL Mutations in Chinese Children Leading to Glycogen Storage Disease Type VI: Two Case Reports
BMC Medical Genetics
Genetics
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