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GJB2 Mutations in Hearing Impairment: Identification of a Broad Clinical Spectrum for Improved Genetic Counseling

The Laryngoscope, 2005-03, Vol.115 (3), p.461-465

2005

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Connexin 26 mutations in cases of sensorineural deafness in eastern Austria

European journal of human genetics : EJHG, 2002-07, Vol.10 (7), p.427-432

2002

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High Incidence of GJB2 Mutations During Screening of Newborns for Hearing Loss in Austria

Ear and hearing, 2007-06, Vol.28 (3), p.298-301

2007

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Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria

Hearing research, 2004-10, Vol.196 (1), p.115-118

2004

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Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria

Hearing research, 2004-08, Vol.194 (1), p.81-86

2004

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A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness

Audiology & neurotology, 2004-01, Vol.9 (1), p.47-50

2004

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Relevance of the A1555G mutation in the 12S rRNA gene for hearing impairment in Austria

Otology & neurotology, 2007-10, Vol.28 (7), p.884

2007

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Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Nature genetics, 1998-05, Vol.19 (1), p.60-62

1998

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Christentum und Naturwissenschaft

Christentum und europäische Kultur, 2023, p.115-130

2, 2023

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Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family

Cytogenetics and cell genetics, 1998, Vol.82 (1-2), p.126

1998

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Ribosomal gene transcription is organized in foci within nucleolar components

Histochemistry and cell biology, 1998-02, Vol.109 (2), p.111-118

1998

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Glucose availability alters ischaemia-induced changes in intracellular pH and calcium of isolated rat spinal roots

Brain research, 1996-06, Vol.725 (1), p.30-36

1996

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A study on nucleolar DNA : isolation of DNA from fibrillar components and ultrastructural localization of different DNA probes

Journal of cell science, 1993-04, Vol.104 (4), p.1199-1205

1993

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Distribution and migration of angiogenic cells from grafted avascular intraembryonic mesoderm

Anatomy and embryology, 1991-01, Vol.183 (4), p.371-377

1991

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GJB2 Mutations in Hearing Impairment: Identification of a Broad Clinical Spectrum for Improved Genetic Counseling

Connexin 26 mutations in cases of sensorineural deafness in eastern Austria

High Incidence of GJB2 Mutations During Screening of Newborns for Hearing Loss in Austria

Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria

Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria

A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness

Relevance of the A1555G mutation in the 12S rRNA gene for hearing impairment in Austria

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Christentum und Naturwissenschaft

Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family

Ribosomal gene transcription is organized in foci within nucleolar components

Glucose availability alters ischaemia-induced changes in intracellular pH and calcium of isolated rat spinal roots

A study on nucleolar DNA : isolation of DNA from fibrillar components and ultrastructural localization of different DNA probes

Distribution and migration of angiogenic cells from grafted avascular intraembryonic mesoderm

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