Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Maria M. van Genderen

Homozygosity Mapping in Patients With Cone–Rod Dystrophy: Novel Mutations and Clinical Characterizations

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2010English

Electroretinogram Abnormalities in Non-Infectious Uveitis Often Persist

Acta Ophthalmologica
MedicineOphthalmology
2020English

Related publications

Novel CDHR1 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Novel C8ORF37 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Cone Dystrophy With Supernormal Rod Response Is Strictly Associated With Mutations inKCNV2

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2008English

Autosomal Dominant Cone-Rod Dystrophy With Negative Electroretinogram.

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
1995English

Spondylometaphyseal Dysplasia-Cone-Rod Dystrophy Syndrome

2020English

Rod-Cone Dystrophy in Spinocerebellar Ataxia Type 1

Archives of Ophthalmology
2011English

Clinical Course of Cone Dystrophy Caused by Mutations in the RPGR Gene

Graefe's Archive for Clinical and Experimental Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2011English

Cone-Rod Dystrophy and Amelogenesis Imperfecta (Jalili Syndrome): Phenotypes and Environs

Eye
MedicineArtsSensory SystemsOphthalmologyHumanities
2010English

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

Acta Ophthalmologica
MedicineOphthalmology
2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy