Whole-exome sequencing - Globe Thesis

Keyword [Whole-exome sequencing] Result: 141 - 160 \| Page: 8 of 10
141.	Mutation Screening And Genetic Study Of Multiple Morphological Abnormalities In The Sperm Flagella
142.	Molecular Genetics And Resting Functional Magnetic Resonance Imaging Of Retinitis Pigmentosa
143.	Preliminary Study On The Clinical And Genetic Causes Of Congenital Bilateral Absence Of Vas Deferens
144.	Correlation Analysis And Pathogenicity Study Of Genes Related To Lumbar Intervertebral Disc Degeneration And Congenital Scoliosis
145.	Genotype Study Of Rheumatoid Arthritis-related Interstitial Lung Diseases
146.	1. Research On The Genetic Characteristics Of Caroli Disease Family�using Whole-exome Sequence Sequencing To Detect PKHD1 Gene Mutation 2. Neuroblastoma And Hepatoblastoma RECK And Related MMPs Expression And Comparative Analysis Of Tumor Metastasis
147.	The Study Of The Correlation Between CAPS Gene Mutation And Recurrent Miscarriage
148.	Study On The Discovery Of A New Pathogenic Gene BMP9 In Idiopathic Pulmonary Hypertension By Whole-exome Sequencing
149.	Genetic Study Of Amyotrophic Lateral Sclerosis 1. Study On The Characteristics Of Gene Mutations In Chinese Patients With Amyotrophic Lateral Sclerosis 2. Study On The Transcriptional Effects Of Amyotrophic Lateral Sclerosis-associated KIF5A Gene Mutation
150.	Research On Genetic Variation Of Several Important Skin-related Diseases
151.	Mutation Screening Of Patients Who Were Born From Related Parents With Multiple Morphological Abnormalities Of The Sperm Flagella
152.	Molecular Mechanism Of Low Energy Metabolism In Kidney�Yang Deficiency Based On Mitochondrial Maternal Inheritance
153.	Identifcation Of Susceptibility Genes In Non-syndromic Cleft Lip With Or Without Cleft Palate Using Whole-exome Sequencing
154.	Whole-exome Sequencing Identifying Candidate Genes Of Coronary Heart Disease In A Chinese Zhuang Population Family
155.	The Relationship Between MLL2 Gene Mutation And The Prognosis Of NK/T Cell Lymphoma
156.	A New Causative Gene ARMC5 Mutation Indentified By Whole-exome Sequencing In Primary Bilateral Macronodular Adrenal Hyperplasia
157.	Primary Cilary Dyskinesia:Report Of Four Case And Review Of The Literature
158.	Whole Exome Sequencing Searches For The Suspicious Pathogenic Gene ADAMTS9 Of Adolescent Idiopathic Scoliosis
159.	Mutations In LRP1 Gene Are Associated With Prostate Cancer In Zhuangs
160.	Clinical Analysis Of Assisted Reproductive Technology With M�llerian Duct Abnormalities Of Assisted Reproductive Technology And Gene Mutation Study
<<First <Prev Next> Last>> Jump to