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Publications by Kaiyan Zhang
Doyne Honeycomb Retinal Dystrophy/Malattia Leventinese Induced by EFEMP1 Mutation in a Chinese Family
BMC Ophthalmology
Medicine
Ophthalmology
Retrograde en Bloc Resection for Non-Muscle Invasive Bladder Tumor Can Reduce the Risk of Seeding Cancer Cells Into the Peripheral Circulation
World Journal of Surgical Oncology
Surgery
Oncology
Related publications
Genetic Testing for Doyne Honeycomb Retinal Dystrophy
The EuroBiotech Journal
Arg555Gln Mutation of TGFBI Gene in Geographical-Type Reis—Bücklers Corneal Dystrophy in a Chinese Family
Journal of International Medical Research
Biochemistry
Medicine
Cell Biology
A Founder Mutation in CERKL Is a Major Cause of Retinal Dystrophy in Finland
Acta Ophthalmologica
Medicine
Ophthalmology
A Possible Novel TGFBI Mutation Ser591Phe in a Finnish Family With Lattice Corneal Dystrophy
Acta Ophthalmologica
Medicine
Ophthalmology
Hereditary Retinal Dystrophy
Mild Cone‐rod Dystrophy and Sensorineural Hearing Loss With CEP250 Mutation in a Japanese Family
Acta Ophthalmologica
Medicine
Ophthalmology
a Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family
G3: Genes, Genomes, Genetics
Medicine
Genetics
Molecular Biology
A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family
BioMed Research International
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
A Novel COL4A4 Mutation Identified in a Chinese Family With Thin Basement Membrane Nephropathy
Scientific Reports
Multidisciplinary