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Publications by Erdmute Kunstmann

Phenotypic Variability of Patients Homozygous for the GJB2 Mutation 35delG Cannot Be Explained by the Influence of One Major Modifier Gene

European Journal of Human Genetics

English

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

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

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

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Hypothesis of the Conjunct Expression Gene: Can Random Mutation Explain the Phenotypic Variability?

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Hemophilia A: Different Phenotypes May Be Explained by Multiple and Variable Effects of the Causative Mutation in the F8 Gene

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A Novel Homozygous Mutation of GJB2—A New Variant of Keratitis-Ichthyosis-Deafness Syndrome?

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Vestibular Dysfunction in the Epistatic Circler Mouse Is Caused by Phenotypic Interaction of One Recessive Gene and Three Modifier Genes

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

Monatsschrift fur Kinderheilkunde

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The Compliance of Clinicians and Patients Cannot Be Globalized

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