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Keyword [syndromic hearing loss]
Result: 41 - 50 | Page: 3 of 3
41. Analysis Of Genotype-Phenotype Correlations In Deafness Syndrome And Exploration Of Early Non-invasive Prenatal Testing Based On Endocervical Fetal Trophoblast
42. Analysis Of Mitochondrial DNA A1555G And C1494T Mutations In 192 Hainan Province Patients With Non-syndromic Hearing Loss
43. Detection And Analysis Of Common Deafness Genes In The North Of Anhui Province
44. Study And Application Of New Diagnostic Techniques On Genetic Deafness Genes And Molecular Genetic Study On A Family With Nonsyndromic Deafness
45. The Study Of Mutation Detection And Function In Rare Hereditary Deafness-causing Genes
46. The Study On Whole Exome Sequencing Of Deafness Gene In Pedigrees Of Non-syndromic Hearing Loss In Guangxi Region
47. Clinical And Genetic Analysis Of Rare Syndromic Hearing Loss
48. Identification Of The Deafness Gene In A Family With X-linked Dominant Non-syndromic Hearing Loss And Studies On The Function In SMPX
49. Genetic Etiology Analysis Of Five Deafness Families And Functional Identification Of A Novel Variant In CDH23 Gene
50. Application Study Of Genetic Diagnosis In Nonsyndromic Hearing Loss By Suspension Array Technology
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