GJB2gene - Globe Thesis

Keyword [GJB2gene] Result: 1 - 16 \| Page: 1 of 1
1.	HRCT Analysis Of Inner Ear Malformation And Deafness Gene Mutations In Chinese Pedigrees With SNHL
2.	Study On Underlying Molecular Mechanisms Of Monoallelic Mutations Of GJB2Gene In Chinese Nonsyndromic Hearing-impaired Patients
3.	Clinical Characteristics Analysis And Phenotype/genotype Correlations Of GJB2in Patients With Non-syndromic Hearing Loss
4.	Analysis Of Common Deafness Genes Mutations In Children With Profound Hearing Impairment And In Patients With Idiopathic Sudden Hearing Loss
5.	The Analysis Of GJB2Gene, GJB3Gene, SLC26A4Gene And Mitochondrial12S RRNA Gene Mutations In Non-syndromic Deafness Patients
6.	Detection Of GJB2Gene Mutation In A Family With Vohwinkel Syndrome
7.	Association Between GJB2Gene Polymorphism And Patients With Psoriasis
8.	Characteristic Analysis Of Frequent Deafness-correlative Genes Mutation In Hui Nationality Patients With Non-syndromic Hearing Loss From Northwest China
9.	Sequence Analysis Of The Upstream Regulation Sequences Of GJB2Based On GJB2235delC Heterozygous Deaf Patients
10.	Epidemiological Investigation Of GJB2Gene Hot-spot Mutation In Deafness Disabled Populations In Beijing And Yangzhou Of China
11.	Sequence Analysis Of The Upstream Regulation Sequences Of GJB2Based On GJB2235DelC Heterozygous Deaf Patients
12.	The Relation Between Congenital Cytomegalovirus Infection Leading To Hearing Loss And Mutation Of GJB2Gene
13.	A Study On The Patients With Nonsyndromic Hearing Impairment Of GJB2Gene Mutations And Kidney Deficiency And Blood Stasis In Kazak And Uyghur In Xinjiang
14.	The Apoptosis-related Gene Differential Expression In The Cochlea Of GJB2Gene Conditional Knockout Mice
15.	Comparison And Analysis Of Common Mutations In Uighur And Han Patients With Non-syndromic Deafness In Xinjiang
16.	Sequencing Analysis Of GJB2in Children With Deafness In Yunnan
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