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Publications by Pei-Pei Hui
Analysis the Pathogenic Gene of 60 Chinese Children With Congenital Hyperinsulinemia
Endocrine Connections
Internal Medicine
Endocrinology
Metabolism
Diabetes
Related publications
A Novel MIP Gene Mutation Analysis in a Chinese Family Affected With Congenital Progressive Punctate Cataract
PLoS ONE
Multidisciplinary
Identification and Functional Analysis of a Novel MIP Gene Mutation Associated With Congenital Cataract in a Chinese Family
PLoS ONE
Multidisciplinary
GPR143 Gene Mutations in Five Chinese Families With X-Linked Congenital Nystagmus
Scientific Reports
Multidisciplinary
Copy Number Variations in the GATA4 , NKX2-5 , TBX5 , BMP4 CRELD1 , and 22q11.2 Gene Regions in Chinese Children With Sporadic Congenital Heart Disease
Journal of Clinical Laboratory Analysis
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
The Association of RAN and RANBP2 Gene Polymerphisms With Wilms Tumor Risk in Chinese Children
Journal of Cancer
Oncology
Mutation Spectrum Analysis of 29 Causative Genes in 43 Chinese Patients With Congenital Hypothyroidism
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Genetic Analysis of the FBXO42 Gene in Chinese Han Patients With Parkinson’s Disease
BMC Neurology
Medicine
Neurology
A Novel Pathogenic Germline Mutation in the Adenomatous Polyposis Coli Gene in a Chinese Family With Familial Adenomatous Coli
Oncotarget
Oncology
Communication Development of Children With Congenital Deafblindness
Japanese Journal of Sign Language Studies
