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Epistatic relationship between Waardenburg Syndrome genes MITF and PAX3

Nature genetics, 1998-03, Vol.18 (3), p.283-286

1998

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Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29

Cell, 2001-01, Vol.104 (1), p.165-172

2001

Volltextzugriff (PDF)

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2

American journal of human genetics, 1994-10, Vol.55 (4), p.685-694

1994

Volltextzugriff (PDF)

Assignment of the gene for a ubiquitin-conjugating enzyme (UBE2I) to human chromosome band 16p13.3 by in situ hybridization

Cytogenetics and cell genetics, 1996, Vol.75 (4), p.222

1996

Volltextzugriff (PDF)

A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus

Human molecular genetics, 1995-12, Vol.4 (12), p.2391-2394

1995

Volltextzugriff (PDF)

Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type I in two families

American journal of human genetics, 1995, Vol.56 (1), p.75-83

1995

Volltextzugriff (PDF)

Epistatic relationship between Waardenburg genes MITF and PAX3

Nature genetics, 1998-03, Vol.18 (3), p.283-286

1998

Volltextzugriff (PDF)

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3

Human molecular genetics, 1995-10, Vol.4 (10), p.1967-1972

1995

Volltextzugriff (PDF)

The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat

Human molecular genetics, 1992-06, Vol.1 (3), p.215-215

1992

Volltextzugriff (PDF)

Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two families

American journal of human genetics, 1995-01, Vol.56 (1), p.75-83

1995

Volltextzugriff (PDF)

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p1603

Human molecular genetics, 1995, Vol.4 (10), p.1967-1972

1995

Volltextzugriff (PDF)

Early platelet dysfunction: an unrecognized role in the acute coagulopathy of trauma

Journal of the American College of Surgeons, 2012-05, Vol.214 (5), p.739

2012

Volltextzugriff (PDF)

CovRS-Regulated Transcriptome Analysis of a Hypervirulent M23 Strain of Group A Streptococcus pyogenes Provides New Insights into Virulence Determinants

Journal of bacteriology, 2015-10, Vol.197 (19), p.3191-3205

2015

Volltextzugriff (PDF)

Genomic Characterization of a Pattern D Streptococcus pyogenes emm53 Isolate Reveals a Genetic Rationale for Invasive Skin Tropicity

Journal of bacteriology, 2016-06, Vol.198 (12), p.1712-1724

2016

Volltextzugriff (PDF)

Phenotypic differentiation of Streptococcus pyogenes populations is induced by recombination-driven gene-specific sweeps

Scientific reports, 2016-11, Vol.6 (1), p.36644-36644, Article 36644

2016

Volltextzugriff (PDF)

Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

American journal of human genetics, 2009-07, Vol.85 (1), p.25-39

2009

Volltextzugriff (PDF)

Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan

BMC medical genetics, 2004-09, Vol.5 (1), p.24-24, Article 24

2004

Volltextzugriff (PDF)

A study of carbonic anhydrase using Mössbauer spectroscopy

Journal of inorganic & nuclear chemistry, 1976, Vol.38 (7), p.1413-1414

1976

Volltextzugriff (PDF)

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Ear, Auditive Nerve, Cochleovestibular Tract, Facial Nerve: Diseases, Semeiology
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Epistatic relationship between Waardenburg Syndrome genes MITF and PAX3

Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2

Assignment of the gene for a ubiquitin-conjugating enzyme (UBE2I) to human chromosome band 16p13.3 by in situ hybridization

A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus

Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type I in two families

Epistatic relationship between Waardenburg genes MITF and PAX3

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3

The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat

Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two families

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p1603

Early platelet dysfunction: an unrecognized role in the acute coagulopathy of trauma

CovRS-Regulated Transcriptome Analysis of a Hypervirulent M23 Strain of Group A Streptococcus pyogenes Provides New Insights into Virulence Determinants

Genomic Characterization of a Pattern D Streptococcus pyogenes emm53 Isolate Reveals a Genetic Rationale for Invasive Skin Tropicity

Phenotypic differentiation of Streptococcus pyogenes populations is induced by recombination-driven gene-specific sweeps

Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan

A study of carbonic anhydrase using Mössbauer spectroscopy

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