Whole‐exome sequencing analysis in 10 families of sporadic microtia with thoracic deformities
نویسندگان
چکیده
منابع مشابه
identification of genes and mutations in 10 iranian families with nsarhl by whole exome sequencing
introduction: with prevalence figures close to 0.2% at birth, hearing loss (hl) is the most frequent sensory impairment in childhood. in developed countries, genetic causes account for more than 60% of congenital hl, most often resulting in non-syndromic deafness, which is usually autosomal recessive. hereditary nonsyndromic hearing loss (nshl) in iran is highly heterogeneous, rendering molecul...
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ژورنال
عنوان ژورنال: Molecular Genetics & Genomic Medicine
سال: 2021
ISSN: 2324-9269,2324-9269
DOI: 10.1002/mgg3.1657