Syndromic - Globe Thesis

Keyword [Syndromic] Result: 1 - 20 \| Page: 1 of 10
1.	The Gene Mapping For A Non-syndromic Autosomal Dominant Deafness Family
2.	Collecting, Characterizing Of The Genetic Resource And Molecular Mapping Of The Relevant Genes For Hereditary Hearing Impairment
3.	The Study Of Molecular Mechanism In Mitochondrial DNA Mutations Related Hearing Loss
4.	Mapping And Postional Cloning The Causative Genes In Chinese Pedigrees With Non-syndromic Hereditary Hearing Impairment
5.	Molecular Epidemiology And Mechanism Study Of Mitochondrial DNA A1555G Mutation In Hearing Impairment
6.	Mutation Screening And Whole Spectrum Mutation Map Drawing Of GJB2 Gene Among Non-syndromic Hearing Impairment Patients
7.	The Clinical Features And Mutation Analysis Of The Responsible Genes For The Syndromic Hearing Impairment
8.	The Study Of The Parental Craniofacial Morphological Feathers In Patients With Sporadic Non-syndromic Cleft Lip And/or Palate
9.	Study And Application Of New Diagnostic Techniques On Deafness Genes And Molecular Epidemiology Of Hot-spot Mutations Among Non-syndromic Hearing Loss Patients In China
10.	Genetic Analysis Of Non-syndromic Hearing Loss And Waardenburg Syndrome
11.	Molecular Mechanism Of Late-onset Nonsyndromic Hearing Loss And Age-related, Aminoglycoside-induced Hearing Loss
12.	Mapping And Positional Cloning The Causative Genes In Chinese Pedigrees With Non-syndromic Hereditary Hearing Impairment
13.	Localization Of Genes For Inherited Skin Diseases And Hearing Loss And Mutational Studies
14.	Molecular Genetic Analysis Of Waardenburg Syndrome And Non-syndromic Hearing Loss
15.	Study Of Molecular Mechanism Of Non-syndromic Hereditary Hearing Loss
16.	The Study Of Copy Number Variation, KCNJ10 Gene Screening And Expression In Patients With Non-syndromic Enlarged Vestibular Aqueduct
17.	GJB2 (Connexin 26) Gene Mutations In 140 Patients Of Hunan Province With NSHL And Intracellular Distribution Of Two Cx26 Mutants In HeLa Cells
18.	Establishment And Application Of Preimplantation Genetic Diagnostic Technique For Hereditary Hearing Loss And Study Of Molecular Mechanism Of Inherited Deafness Pedigrees
19.	Mutation Screening And Functional Analysis On The Molecular Pathogenesis Of Non-syndromic Tooth Agenesis
20.	Identification Of The Causative CNVs In Syndromic Congenital Heart Defects By High Resolution Array-SNP
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