[HTML][HTML] Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation
T Parzefall, A Frohne, M Koenighofer… - European Archives of …, 2017 - Springer
Bi-allelic variations in the gap junction protein beta-2 (GJB2) gene cause up to 50% of cases
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …
Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation
T Parzefall, A Frohne, M Koenighofer… - … archives of oto …, 2017 - pubmed.ncbi.nlm.nih.gov
Bi-allelic variations in the gap junction protein beta-2 (GJB2) gene cause up to 50% of cases
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …
Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.
T Parzefall, A Frohne, M Koenighofer… - … Archives of Oto …, 2017 - search.ebscohost.com
Bi-allelic variations in the gap junction protein beta-2 (GJB2) gene cause up to 50% of cases
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …
[HTML][HTML] Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation
T Parzefall, A Frohne, M Koenighofer… - European Archives of …, 2017 - ncbi.nlm.nih.gov
Bi-allelic variations in the gap junction protein beta-2 (GJB2) gene cause up to 50% of cases
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …
Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.
T Parzefall, A Frohne, M Koenighofer… - European Archives of …, 2017 - europepmc.org
Bi-allelic variations in the gap junction protein beta-2 (GJB2) gene cause up to 50% of cases
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …
Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.
T Parzefall, A Frohne, M Koenighofer… - European Archives of …, 2017 - europepmc.org
Bi-allelic variations in the gap junction protein beta-2 (GJB2) gene cause up to 50% of cases
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …
of newborn hearing loss. Heterozygous pathogenic GJB2 variations are also fivefold …