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Publications by Yongheng Dou
A Novel FBN2 Mutation Cosegregates With Congenital Contractural Arachnodactyly in a Five-Generation Chinese Family
Clinical Case Reports
Medicine
Related publications
A Novel Splicing Mutation in the FBN2 Gene in a Family With Congenital Contractural Arachnodactyly
Frontiers in Genetics
Genetics
Molecular Medicine
Identification of a Novel Missense FBN2 Mutation in a Chinese Family With Congenital Contractural Arachnodactyly Using Exome Sequencing
PLoS ONE
Multidisciplinary
Mutation Analysis of Fibrillin-2 (FBN2) and Microfibril Associated Protein-3 (MFAP-3): Two Genes Associated With Congenital Contractural Arachnodactyly (CCA), Also Known as Beal's Syndrome
A Novel MIP Gene Mutation Analysis in a Chinese Family Affected With Congenital Progressive Punctate Cataract
PLoS ONE
Multidisciplinary
Contractural Arachnodactyly Versus Marfan's Syndrome.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Targeted Next-Generation Sequencing Identified a Novel ANK1 Mutation Associated With Hereditary Spherocytosis in a Chinese Family
Hematology
Hematology
Identification and Functional Analysis of a Novel MIP Gene Mutation Associated With Congenital Cataract in a Chinese Family
PLoS ONE
Multidisciplinary
Two Novel NPHS1 Mutations in a Chinese Family With Congenital Nephrotic Syndrome
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
Identification of a Novel TCOF1 Mutation in a Chinese Family With Treacher Collins Syndrome
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
