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Publications by Houfa Yin

Identification and Functional Analysis of a Novel MIP Gene Mutation Associated With Congenital Cataract in a Chinese Family

Multidisciplinary

English

Cytokine Profiling Reveals Increased Serum Inflammatory Cytokines in Idiopathic Choroidal Neovascularization

English

Related publications

A Novel MIP Gene Mutation Analysis in a Chinese Family Affected With Congenital Progressive Punctate Cataract

Multidisciplinary

English

Identification of a Novel Missense FBN2 Mutation in a Chinese Family With Congenital Contractural Arachnodactyly Using Exome Sequencing

Multidisciplinary

English

Identification of a Novel Frameshift Mutation in PITX2 Gene in a Chinese Family With Axenfeld-Rieger Syndrome

Journal of Zhejiang University: Science B

Molecular Biology

English

Identification of a Novel TCOF1 Mutation in a Chinese Family With Treacher Collins Syndrome

Experimental and Therapeutic Medicine

Cancer Research

English

Identification of aCRYABMutation Associated With Autosomal Dominant Posterior Polar Cataract in a Chinese Family

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

Sensory Systems

English

A Novel FBN2 Mutation Cosegregates With Congenital Contractural Arachnodactyly in a Five-Generation Chinese Family

Clinical Case Reports

English

A Novel Splicing Mutation in the FBN2 Gene in a Family With Congenital Contractural Arachnodactyly

Frontiers in Genetics

Molecular Medicine

English

A Novel Mutation in the Connexin 46 Gene Causes Autosomal Dominant Congenital Cataract With Incomplete Penetrance

Journal of Medical Genetics

English

Obesity Associated With a Novel Mitochondrial tRNACys 5802A>G Mutation in a Chinese Family

Bioscience Reports

Molecular Biology

English