Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Fanlin Hong

Doyne Honeycomb Retinal Dystrophy/Malattia Leventinese Induced by EFEMP1 Mutation in a Chinese Family

BMC Ophthalmology

English

Related publications

Genetic Testing for Doyne Honeycomb Retinal Dystrophy

The EuroBiotech Journal

English

Arg555Gln Mutation of TGFBI Gene in Geographical-Type Reis—Bücklers Corneal Dystrophy in a Chinese Family

Journal of International Medical Research

English

A Founder Mutation in CERKL Is a Major Cause of Retinal Dystrophy in Finland

Acta Ophthalmologica

English

A Possible Novel TGFBI Mutation Ser591Phe in a Finnish Family With Lattice Corneal Dystrophy

Acta Ophthalmologica

English

Hereditary Retinal Dystrophy

English

Mild Cone‐rod Dystrophy and Sensorineural Hearing Loss With CEP250 Mutation in a Japanese Family

Acta Ophthalmologica

English

a Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family

G3: Genes, Genomes, Genetics

Molecular Biology

English

A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family

BioMed Research International

Molecular Biology

English

A Novel COL4A4 Mutation Identified in a Chinese Family With Thin Basement Membrane Nephropathy

Scientific Reports

Multidisciplinary

English