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Keyword [USH2A]
Result: 1 - 12 | Page: 1 of 1
1.
The Clinical Features And Mutation Analysis Of The Responsible Genes For The Syndromic Hearing Impairment
2.
The Molecular Genetics Research Of Retinitis Pigmentosa/Usher Syndrom Pedigree
3.
The Phenotype And Genotype Of Spontaneous Hereditary Retinitis Pigmentosa/deafness Mouse Models
4.
Genetic Screening Of Mutation For Patients With Non-syndromic Hearing Loss And Pathogenic Site Analysis In The Deafness Family With Usher Syndrome
5.
Novel Mutations In The USH2A Gene In A Family Affected With Usher Syndrome Type2
6.
Knockout Of USH2A Gene In Zebrafish Causes Hearing Impairment And Late Onset Rod-cone Dystrophy
7.
Knockout Of USH2A Gene In Zebrafish Causes Hearing Impairment And Late Onset Rod-Cone Dystrophy
8.
Phenotype And Genotype Analysis Of USH2A Gene Related Hereditary Retinal Diseases
9.
Identification Of Pathogenic Genes In Four Patients With Usher Syndrome And A Preliminary Phenotype Observation In Ush2a Knockout Mice
10.
Pathogenic Genes Analysis In Two Multigenerational Chinese Families With Autosomal Predominant High Myopia
11.
Identification Of The Causative Genes For A Family With Usher Syndrome And The Meta Analysis Of Epidemiological Studies In Usher Syndrome
12.
Clinical And Genetic Characteristics Of USH2A-associated Nonsyndromic Retinitis Pigmentosa And Usher Syndrome Type Ⅱ
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