Prevalence of congenital hereditary sensorineural deafness in Australian Cattle Dogs and associations with coat characteristics and sex
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1746-6148
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Prevalence of congenital hereditary sensorineural deafness in Australian Cattle Dogs and associations with coat characteristics and sex ; volume:8 ; number:1 ; day:29 ; month:10 ; year:2012 ; pages:1-16 ; date:12.2012
BMC veterinary research ; 8, Heft 1 (29.10.2012), 1-16, 12.2012
- Urheber
-
Sommerlad, Susan F.
- Beteiligte Personen und Organisationen
-
Morton, John M.
Haile-Mariam, Mekonnen
JOHNSTONE, ISOBEL
Seddon, Jennifer M.
O’Leary, Caroline A.
SpringerLink (Online service)
- DOI
-
10.1186/1746-6148-8-202
- URN
-
urn:nbn:de:1111-2016080548793
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 11:00 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Sommerlad, Susan F.
- Morton, John M.
- Haile-Mariam, Mekonnen
- JOHNSTONE, ISOBEL
- Seddon, Jennifer M.
- O’Leary, Caroline A.
- SpringerLink (Online service)
Ähnliche Objekte (12)
Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)
Molecular genetic analysis of canine congenital sensorineural deafness in Dalmatian dogs
Prevalence, heritability and genetic correlations of congenital sensorineural deafness and coat pigmentation phenotype in the English bull terrier
Deafness-in-a-dish: modeling hereditary deafness with inner ear organoids
Congenital sensorineural deafness in client owned pure breed white cats
De-novo and genome-wide meta-analyses identify a risk haplotype for congenital sensorineural deafness in Dalmatian dogs
Possible mechanisms for sensorineural hearing loss and deafness in patients with propionic acidemia
Molecular genetic analysis of congenital deafness in Dalmatian dogs
AAV‐mediated Gene Therapy for Hereditary Deafness: Progress and Perspectives
MPZL2—a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population
The pathogenesis of common Gjb2 mutations associated with human hereditary deafness in mice
The importance of cochlear nerve canal for the preoperative evaluation of children with high grade sensorineural hearing loss or deafness
Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)
Molecular genetic analysis of canine congenital sensorineural deafness in Dalmatian dogs
Prevalence, heritability and genetic correlations of congenital sensorineural deafness and coat pigmentation phenotype in the English bull terrier
Deafness-in-a-dish: modeling hereditary deafness with inner ear organoids
Congenital sensorineural deafness in client owned pure breed white cats
De-novo and genome-wide meta-analyses identify a risk haplotype for congenital sensorineural deafness in Dalmatian dogs
Possible mechanisms for sensorineural hearing loss and deafness in patients with propionic acidemia
Molecular genetic analysis of congenital deafness in Dalmatian dogs
AAV‐mediated Gene Therapy for Hereditary Deafness: Progress and Perspectives
MPZL2—a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population
The pathogenesis of common Gjb2 mutations associated with human hereditary deafness in mice
The importance of cochlear nerve canal for the preoperative evaluation of children with high grade sensorineural hearing loss or deafness
Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)
Molecular genetic analysis of canine congenital sensorineural deafness in Dalmatian dogs
Prevalence, heritability and genetic correlations of congenital sensorineural deafness and coat pigmentation phenotype in the English bull terrier
Deafness-in-a-dish: modeling hereditary deafness with inner ear organoids
Congenital sensorineural deafness in client owned pure breed white cats
De-novo and genome-wide meta-analyses identify a risk haplotype for congenital sensorineural deafness in Dalmatian dogs
Possible mechanisms for sensorineural hearing loss and deafness in patients with propionic acidemia
Molecular genetic analysis of congenital deafness in Dalmatian dogs
AAV‐mediated Gene Therapy for Hereditary Deafness: Progress and Perspectives
MPZL2—a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population
The pathogenesis of common Gjb2 mutations associated with human hereditary deafness in mice