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Publications by L Van Laer

A Common Founder for the 35delG GJB2 Gene Mutation in Connexin 26 Hearing Impairment

Journal of Medical Genetics

English

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Frequency of C.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients With Nonsyndromic Hearing Impairment

Genetics Research International

Molecular Biology

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Unauffälliges UNHS-Screening Bei Einem Homozygoten Träger Der 35delG-Mutation Im Connexin 26 Kodierenden Gjb2-Gen

Monatsschrift fur Kinderheilkunde

English

A Novel Splice-Site Mutation in the GJB2 Gene Causing Mild Postlingual Hearing Impairment

Multidisciplinary

English

Rapid Detection of the 35delG Mutation in the GJB2 Gene in Childhood Deafness

Journal of Medical Screening

Occupational Health

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Recurrent Mutations in the Deafness Gene GJB2 (Connexin 26) in British Asian Families

Journal of Medical Genetics

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Connexin 26 (GJB2) Gene-Related Deafness and Speech Intelligibility After Cochlear Implantation

Otology and Neurotology

Otorhinolaryngology

Sensory Systems

English

Mutations of the Connexin 26 Gene in Families With Non-Syndromic Hearing Loss

Molecular Medicine Reports

Molecular Biology

Cancer Research

Molecular Medicine

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KID Syndrome: Report of a Scandinavian Patient With Connexin‐26 Gene Mutation

Acta Dermato-Venereologica

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A Common Founder Mutation in the EDA-A1 Gene in X-Linked Hypodontia

English