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Keyword [Usher Syndrome]
Result: 1 - 20 | Page: 1 of 2
1. The Clinical Features And Mutation Analysis Of The Responsible Genes For The Syndromic Hearing Impairment
2. Analysis Of Clinical Features And Study Of Responsible Genes For The Chinese Retinitis Pigmentosa And Usher Syndrome Families
3. Whirlin Interacts With Espin And Modulates Its Actin-regulatory Function
4. Genetic And Clinical Analysis Of Usher Syndrome And Stargardt Disease In Patients Of Southwest China
5. Identification Of The Genetic Basis For A Chinese Families Associated With Usher Syndrome
6. Molecular Mechanism Of Very Large G Protein Coupled Receptor (VLGR1) Signal Transduction And Its Function
7. Identification Of The Causative Genes For A Chinese Family With Autosomal Dominant Hereditary Hearing Loss And A Sporadic Case Of Usher Syndrome
8. Identification Of CDH23 Mutation In A Family With Usher Syndrome
9. The Phenotype And Genotype Of Spontaneous Hereditary Retinitis Pigmentosa/deafness Mouse Models
10. Identify Pathogenic Variant For Usher Syndrome By Wholeexome Sequencing
11. Genetic Screening Of Mutation For Patients With Non-syndromic Hearing Loss And Pathogenic Site Analysis In The Deafness Family With Usher Syndrome
12. Novel Mutations In The USH2A Gene In A Family Affected With Usher Syndrome Type2
13. Knockout Of USH2A Gene In Zebrafish Causes Hearing Impairment And Late Onset Rod-cone Dystrophy
14. Investigation Of Animal Models For Retinitis Pigmentosa And The Effects Of Molecular Hydrogen On Them
15. Knockout Of USH2A Gene In Zebrafish Causes Hearing Impairment And Late Onset Rod-Cone Dystrophy
16. Study On The Mechanism Of Interaction Between Espin And Whirlin
17. Phenotype And Genotype Analysis Of USH2A Gene Related Hereditary Retinal Diseases
18. Analysis Of PCDH15 Gene Mutation And Prenatal Diagnosis In A Pedigree Affected With Usher Syndrome Type 1
19. Identification Of Pathogenic Genes In Four Patients With Usher Syndrome And A Preliminary Phenotype Observation In Ush2a Knockout Mice
20. Clinical Characteristics And Molecular Etiology Of Common Syndromic Deafness With Ocular Abnormalities
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