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Publications by Elfride De Baere

Correction: Mapping the Genomic Landscape of Inherited Retinal Disease Genes Prioritizes Genes Prone to Coding and Noncoding Copy-Number Variations

Genetics in Medicine
MedicineGenetics
2018English

ABCA4-associated Disease as a Model for Missing Heritability in Autosomal Recessive Disorders: Novel Noncoding Splice, Cis-Regulatory, Structural, and Recurrent Hypomorphic Variants

Genetics in Medicine
MedicineGenetics
2019English

In This Issue

Genetics in Medicine
MedicineGenetics
2012English

Early-Onset Autosomal Recessive Cerebellar Ataxia Associated With Retinal Dystrophy: New Human Hotfoot Phenotype Caused by Homozygous GRID2 Deletion

Genetics in Medicine
MedicineGenetics
2014English

Under-Reported Aspects of Diagnosis and Treatment Addressed in the Dutch-Flemish Guideline for Comprehensive Diagnostics in Disorders/Differences of Sex Development

Journal of Medical Genetics
Genetics
2020English

Extensive Clinical, Hormonal and Genetic Screening in a Large Consecutive Series of 46,XY Neonates and Infants With Atypical Sexual Development

Orphanet Journal of Rare Diseases
MedicineGeneticsPharmacology
2014English

Ethical Values Supporting the Disclosure of Incidental and Secondary Findings in Clinical Genomic Testing: A Qualitative Study

BMC Medical Ethics
Health PolicyEthicsHealthIssuesLegal Aspects
2020English

Disease-Causing 7.4 Kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction With the FOXL2 Promotor: Implications for Mutation Screening

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2009English

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