Clinical Phenotype - Globe Thesis

Keyword [Clinical Phenotype] Result: 141 - 160 \| Page: 8 of 9
141.	Study On The Clinical Phenotype And Immune Metabolism Characteristics Of Mevalonate Kinase Deficiency
142.	Clinical Phenotype Data And Lipid Peroxidation Study Of Non-alcoholic Fatty Liver Disease With Accumulation Of Damp-heat
143.	Mutation Gene Detection And Clinical Phenotype Analysis Of A Family Of VHL Syndrome
144.	Research On The Phenomenon That The Clinical Phenotype Of Pemphigus Does Not Correspond To The Antibody Profile
145.	Genetic Diagnosis Study Of Male Congenital Bilateral Absent Vas Deferens
146.	Anhedonia in Major Depressive Disorder: Exploration of a Predictive Clinical Phenotype
147.	Clinical Phenotype Of Patients With PCOS Between North And South And The Adberse Events About PCOSAct Project
148.	Study On The Predictive Value Of Clinical Phenotypic Characteristics Combined With Inflammatory Biomarkers For Delirium In Critically Ill Children And Symptom Management Strategies
149.	Analysis Of The Correlation Between HLA Allele And Clinical Phenotype And Prognosis Of Children With Primary Nephrotic Syndrome
150.	Classification Of MAFLD Subtypes Based On TCM Clinical Phenotype And Oral-intestinal Flora Characteristics Of Obese-MAFLD
151.	Relation Between Sex Hormone Binding Globulin And Clinical Phenotypes In Type 2 Diabetes Mellitus
152.	Genotype,Clinical Phenotype And Spermatogenesis In Patients With Congenital Hypogonadotropic Hypogonadism(CHH),Focusing On Gene Mutation Of FGFR1
153.	Analysis Of Clinical Features And Gene Mutation Sites In 116 Patients With Wilson's Disease
154.	Clinical Analysis Of Spinal Muscular Atrophy Types 1-2 In 56 Children
155.	Analysis Of Talaromycosis In Children With Primary Immunodeficiencies Based On Clinical Phenotype And Genotype
156.	Clinical Features And Genetic Characteristics Of Hereditary Diffuse Leukoencephalopathy With Spheroids Due To CSF1R Mutations
157.	Clinical Manifestation And Genetic Analysis Of 165 Children With Suspected Genetic Epilepsy
158.	Retrospective Analysis And Follow-up Of Myelin Oligodendrocyte Glycoprotein Antibody-associated Disorders In Childhood
159.	Clinical Phenotype Analysis And Primary Pathogenesis Discussion Of MYH7 Gene Mutations Related Cardiomyopathy In Children
160.	Analysis Of Clinical Phenotype And Genetic Etiology Of A Family With Pulmonary Atresia
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