[HTML][HTML] Identification of SLC26A4 c. 919-2A> G compound heterozygosity in hearing-impaired patients to improve genetic counseling
Q Li, Q Zhu, Y Yuan, S Huang, D Han, D Huang… - Journal of Translational …, 2012 - Springer
Background Mutations in the SLC26A4 gene, which encodes the anion transporter, pendrin,
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
[HTML][HTML] Identification of SLC26A4 c. 919-2A> G compound heterozygosity in hearing-impaired patients to improve genetic counseling
Q Li, Q Zhu, Y Yuan, S Huang… - Journal of …, 2012 - … -medicine.biomedcentral.com
Mutations in the SLC26A4 gene, which encodes the anion transporter, pendrin, are a major
cause of autosomal recessive non-syndromic hearing loss (NSHL) in some Asian …
cause of autosomal recessive non-syndromic hearing loss (NSHL) in some Asian …
Identification of SLC26A4 c. 919-2A> G compound heterozygosity in hearing-impaired patients to improve genetic counseling.
Q Li, Q Zhu, Y Yuan, S Huang, D Han… - Journal of …, 2012 - search.ebscohost.com
Background: Mutations in the SLC26A4 gene, which encodes the anion transporter, pendrin,
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
Identification of SLC26A4 c. 919-2A> G compound heterozygosity in hearing-impaired patients to improve genetic counseling.
Q Li, QW Zhu, YY Yuan, SS Huang, DY Han… - Journal of …, 2012 - europepmc.org
Background Mutations in the SLC26A4 gene, which encodes the anion transporter, pendrin,
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
[HTML][HTML] Identification of SLC26A4 c. 919-2A> G compound heterozygosity in hearing-impaired patients to improve genetic counseling
Q Li, Q Zhu, Y Yuan, S Huang, D Han… - Journal of …, 2012 - ncbi.nlm.nih.gov
Background Mutations in the SLC26A4 gene, which encodes the anion transporter, pendrin,
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
[PDF][PDF] Identification of SLC26A4 c. 919-2A> G compound heterozygosity in hearing-impaired patients to improve genetic counseling
Q Li, Q Zhu, Y Yuan, S Huang, D Han, D Huang, P Dai - 2012 - cyberleninka.org
Background: Mutations in the SLC26A4 gene, which encodes the anion transporter, pendrin,
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
[PDF][PDF] Identification of SLC26A4 c. 919-2A> G compound heterozygosity in hearing-impaired patients to improve genetic counseling
Q Li, Q Zhu, Y Yuan, S Huang, D Han, D Huang, P Dai - 2012 - scienceopen.com
Background: Mutations in the SLC26A4 gene, which encodes the anion transporter, pendrin,
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
Identification of SLC26A4 c. 919-2A> G compound heterozygosity in hearing-impaired patients to improve genetic counseling
Q Li, Q Zhu, Y Yuan, S Huang, D Han… - Journal of Translational …, 2012 - go.gale.com
Background Mutations in the SLC26A4 gene, which encodes the anion transporter, pendrin,
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
Identification of SLC26A4 c. 919-2A> G compound heterozygosity in hearing-impaired patients to improve genetic counseling
Q Li, Q Zhu, Y Yuan, S Huang… - Journal of …, 2012 - pubmed.ncbi.nlm.nih.gov
Background Mutations in the SLC26A4 gene, which encodes the anion transporter, pendrin,
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
are a major cause of autosomal recessive non-syndromic hearing loss (NSHL) in some …
Identification of SLC26A4 c. 919-2A> G compound heterozygosity in hearing-impaired patients to improve genetic counseling
Q Li, Q Zhu, Y Yuan, S Huang, D Han… - Journal of …, 2012 - search.proquest.com
Mutations in the SLC26A4 gene, which encodes the anion transporter, pendrin, are a major
cause of autosomal recessive non-syndromic hearing loss (NSHL) in some Asian …
cause of autosomal recessive non-syndromic hearing loss (NSHL) in some Asian …