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Publications by Karen Brondum-Nielsen
Birth Prevalence and Mutation Spectrum in Danish Patients With Autosomal Recessive Albinism
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Severe Male Infertility. Impact of Genetic Factors on Diagnosis and Counselling
Acta Obstetricia et Gynecologica Scandinavica
Medicine
Gynecology
Obstetrics
Related publications
Albinism, a Semi-Lethal Autosomal Mutation in Lebistes Reticulatus
Heredity
Genetics
High Prevalence of Mutations in theEYSGene in Japanese Patients With Autosomal Recessive Retinitis Pigmentosa
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Mutations in USH2A in Spanish Patients With Autosomal Recessive Retinitis Pigmentosa: High Prevalence and Phenotypic Variation
Journal of Medical Genetics
Genetics
Mutation Screening of Multiple Genes in Spanish Patients With Autosomal Recessive Retinitis Pigmentosa by Targeted Resequencing
PLoS ONE
Multidisciplinary
A Novel NR2E3 Gene Mutation in Autosomal Recessive Retinitis Pigmentosa With Cystic Maculopathy
Acta Ophthalmologica
Medicine
Ophthalmology
Mutation in Kallikrein 4 Causes Autosomal Recessive Hypomaturation Amelogenesis Imperfecta
Journal of Medical Genetics
Genetics
Mutation in the Intracellular Chloride Channel CLCC1 Associated With Autosomal Recessive Retinitis Pigmentosa
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Screening of the Connexin 26 (35delg) Mutation in Egyptian Patients With Autosomal Recessive Nonsyndromic Deafness and Its Relation to the Patients' Iq
Egyptian Journal of Genetics and Cytology
Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss
Zahedan Journal of Research in Medical Sciences
