Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province
Y Zhou, C Li, M Li, Z Zhao, S Tian, H Xia… - … Genetics & Genomic …, 2019 - Wiley Online Library
Background Hearing impairment is one of most frequent birth defects, which affects nearly 1
in every 1,000 live births. However, the molecular etiology of non‐syndromic deafness in …
in every 1,000 live births. However, the molecular etiology of non‐syndromic deafness in …
[HTML][HTML] Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province
Y Zhou, C Li, M Li, Z Zhao, S Tian, H Xia… - Molecular Genetics & …, 2019 - ncbi.nlm.nih.gov
Background Hearing impairment is one of most frequent birth defects, which affects nearly 1
in every 1,000 live births. However, the molecular etiology of non‐syndromic deafness in …
in every 1,000 live births. However, the molecular etiology of non‐syndromic deafness in …
Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province.
Y Zhou, C Li, M Li, Z Zhao, S Tian… - Molecular Genetics …, 2019 - search.ebscohost.com
Background: Hearing impairment is one of most frequent birth defects, which affects nearly 1
in every 1,000 live births. However, the molecular etiology of non‐syndromic deafness in …
in every 1,000 live births. However, the molecular etiology of non‐syndromic deafness in …
Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province
Y Zhou, C Li, M Li, Z Zhao, S Tian, H Xia, P Liu… - Molecular Genetics & …, 2019 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: sec>< jats: title> Background</jats: title>< jats: p>
Hearing impairment is one of most frequent birth defects, which affects nearly 1 in every …
Hearing impairment is one of most frequent birth defects, which affects nearly 1 in every …
Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province
Y Zhou, C Li, M Li, Z Zhao, S Tian, H Xia… - Molecular Genetics …, 2019 - search.proquest.com
Background Hearing impairment is one of most frequent birth defects, which affects nearly 1
in every 1,000 live births. However, the molecular etiology of non‐syndromic deafness in …
in every 1,000 live births. However, the molecular etiology of non‐syndromic deafness in …
Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province
Y Zhou, C Li, M Li, Z Zhao, S Tian… - Molecular genetics …, 2019 - pubmed.ncbi.nlm.nih.gov
Background Hearing impairment is one of most frequent birth defects, which affects nearly 1
in every 1,000 live births. However, the molecular etiology of non-syndromic deafness in …
in every 1,000 live births. However, the molecular etiology of non-syndromic deafness in …
Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province.
Y Zhou, C Li, M Li, Z Zhao, S Tian, H Xia… - Molecular Genetics & …, 2019 - europepmc.org
Background Hearing impairment is one of most frequent birth defects, which affects nearly 1
in every 1,000 live births. However, the molecular etiology of non-syndromic deafness in …
in every 1,000 live births. However, the molecular etiology of non-syndromic deafness in …
Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province.
Y Zhou, C Li, M Li, Z Zhao, S Tian, H Xia… - Molecular Genetics & …, 2019 - europepmc.org
Background Hearing impairment is one of most frequent birth defects, which affects nearly 1
in every 1,000 live births. However, the molecular etiology of non-syndromic deafness in …
in every 1,000 live births. However, the molecular etiology of non-syndromic deafness in …