C.35delG/ GJB2 and del(GJB6-D13S1830) mutations in Croatians with prelingual non-syndromic hearing impairment

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1472-6815

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: C.35delG/ GJB2 and del(GJB6-D13S1830) mutations in Croatians with prelingual non-syndromic hearing impairment ; volume:5 ; number:1 ; day:08 ; month:12 ; year:2005 ; pages:1-4 ; date:12.2005
BMC ear, nose and throat disorders ; 5, Heft 1 (08.12.2005), 1-4, 12.2005

Creator: Medica, Igor

Contributor: Rudolf, Gorazd
Balaban, Manuela
Peterlin, Borut
SpringerLink (Online service)

DOI: 10.1186/1472-6815-5-11

URN: urn:nbn:de:1111-2016071626814

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:53 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Medica, Igor
Rudolf, Gorazd
Balaban, Manuela
Peterlin, Borut
SpringerLink (Online service)

Other Objects (12)

THBS1 is a new autosomal recessive non-syndromic hearing impairment gene

Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families

Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment

A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment

OR11-002 - Mutations in MVK cause non-syndromic RP

Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients

DNA methylation in hearing-related genes in non-syndromic sensorineural hearing loss patients

Copy number variants are a common cause of non-syndromic hearing loss

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria

THBS1 is a new autosomal recessive non-syndromic hearing impairment gene

Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families

Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment

A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment

OR11-002 - Mutations in MVK cause non-syndromic RP

Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients

DNA methylation in hearing-related genes in non-syndromic sensorineural hearing loss patients

Copy number variants are a common cause of non-syndromic hearing loss

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria

THBS1 is a new autosomal recessive non-syndromic hearing impairment gene

Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families

Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment

A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment

OR11-002 - Mutations in MVK cause non-syndromic RP

Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients

DNA methylation in hearing-related genes in non-syndromic sensorineural hearing loss patients

Copy number variants are a common cause of non-syndromic hearing loss

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

C.35delG/ GJB2 and del(GJB6-D13S1830) mutations in Croatians with prelingual non-syndromic hearing impairment

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

THBS1 is a new autosomal recessive non-syndromic hearing impairment gene

Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families

Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment

A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment

OR11-002 - Mutations in MVK cause non-syndromic RP

Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients

DNA methylation in hearing-related genes in non-syndromic sensorineural hearing loss patients

Copy number variants are a common cause of non-syndromic hearing loss

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria

THBS1 is a new autosomal recessive non-syndromic hearing impairment gene

Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families

Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment

A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment

OR11-002 - Mutations in MVK cause non-syndromic RP

Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients

DNA methylation in hearing-related genes in non-syndromic sensorineural hearing loss patients

Copy number variants are a common cause of non-syndromic hearing loss

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria

THBS1 is a new autosomal recessive non-syndromic hearing impairment gene

Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families

Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment

A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment

OR11-002 - Mutations in MVK cause non-syndromic RP

Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients

DNA methylation in hearing-related genes in non-syndromic sensorineural hearing loss patients

Copy number variants are a common cause of non-syndromic hearing loss

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria

Related objects

Reset password