Genetic diagnosis - Globe Thesis

Keyword [Genetic diagnosis] Result: 181 - 200 \| Page: 10 of 10
181.	The development of a decision aid for at-risk couples considering preimplantation genetic diagnosis: Reproductive options: Is PGD right for me
182.	Adult onset genetic disorders and preimplantation genetic diagnosis: Creating educational brochures for those considering family planning
183.	Reflections on the law and ethics of regulating preimplantation genetic diagnosis in the United Kingdom
184.	A Health Policy Ethics Approach Developing Recommendations for Regulation of Preimplantation Genetic Diagnosis in Canada
185.	Establishing A Genetic Diagnosis System For 46, XY DSD And Analyzing Gene Mutation For 46, XY Female /AIS/5α-RD2 Deficiency
186.	The Role Of Nanobacteria In The Pathogenesis Of Type Ⅲ Prostatitis And The Reseach Of Specific Genetic Diagnosis
187.	Polygenic Determinants Of Parkinson’s Disease And The Establishment Of Autosomal Dominant Parkinson’s Disease Genetic Diagnosis Platform
188.	The Establishment Of Genetic Diagnosis Platform For Hereditary Cerebellar Ataxia And Mapping And Cloning Of Novel Causative Genes For Hereditary Cerebellar Ataxia
189.	Application Of Genetic Testing In The Diagnosis Of Diffuse Cystic Lung Disease
190.	Genetic Diagnosis Of F13 Factor Deficiency And The Pathogenesis Of F13A1 Gene Deep Intron Mutation
191.	Prognostic,Genetic Diagnosis Of FSGS And Functional Study Of ADCK4
192.	Study On Application Of CNV-seq In Genetic Diagnosis Of NT Thickening Fetus
193.	The Study On Preimplantation Genetic Diagnosis And Birth Defect Prevention For Polycystic Kidney Disease
194.	Clinical Data Analysis Of Children With Alport Syndrome In A Single Center And Induction Of Pluripotent Stem Cells In A Child With COL4A5 Gene Mutation
195.	Analysis Of Clinical Features And Genetic Diagnosis Of Three Families With Waardengburg Syndrome
196.	Study On Molecular Genetic Pathogenic Factors And Genetic Counseling In Families With Non-syndromic Hereditary Deafness
197.	Clinical Analysis And Genetic Diagnosis Of A Child With Neurofibroma Type 1 Complicated With Juvenile Xanthogranuloma
198.	Application Of Next Generation Sequencing Technology In Analysis Of Gene Mutation Types Of Thalassemia In Rucheng County,Hunan Province
199.	A Study Of Hearing And Speech Influencing Factors And Objective Evaluation In The Cochlear Implant User With Auditory Neuropathy
200.	Diagnostic Yield Of Whole-Exome Sequencing And Identification Of Candidate Genes In Fetuses With Conotruncal Defects
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