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Publications by Katrien Ketelslagers

Bi-Allelic Inactivating Variants in the COCH Gene Cause Autosomal Recessive Prelingual Hearing Impairment

European Journal of Human Genetics

English

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Bi-Allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex

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A NovelESRRBDeletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment Among Pakistani Families

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Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss

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Genotype-Phenotype Correlation Analysis of MYO15A Variants in Autosomal Recessive Non-Syndromic Hearing Loss

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Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

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Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

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Bi-Allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes

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Prevalence of Cx26 (GJB2) Gene Mutations Causing Recessive Nonsyndromic Hearing Impairment in India

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Respiratory Changes During Reading in Mandarin-Speaking Adolescents With Prelingual Hearing Impairment

Folia Phoniatrica et Logopaedica

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