Clinical Phenotype - Globe Thesis

Keyword [Clinical Phenotype] Result: 61 - 80 \| Page: 4 of 9
61.	A Study In The Differential Diagnosis Strategy Of Genes Associated With PSP
62.	Phenotype-genotype Correlations In Patients With Wilson’s Disease
63.	Genotype And Clinical Phenotype In Classical 21-Hydroxylase Deficiency Patients
64.	Genetic Analysis For A Family With Limb-Girdle Muscular Dystrophy
65.	Analysis The Characteristics Of Genetic Mutation And Clinical Manifestations In Familial Alzheimer’s Disease Associated With A Novel PSEN2 Mutation
66.	Association Study Of HTR3A,HTR3B SNP With Schizophrania And Clinical Phenotype
67.	Relevant Research About Plasma Cytokines Expression And The Clinical Phenotype And Drug Resistance In Tb Patients
68.	Analysis Of The Clinical Phenotype And Investigation Of Pathogenic Gene In A Chinese Han Family With Punctate Palmoplantar Keratoderma
69.	The Association Of Systemic Lupus Erythematosus And Its Clinical Phenotype With Multiple Candidate Gene Locus
70.	Analysis Of Clinical Phenotype And Prognostic Factors Of Erythrodermic Psoriasis
71.	Initation Coden Mutation Of ?2-Globin Gene Causing ?-Thalassemia
72.	Study On The Correlation Between Clinical Phenotype And TCM Constitution Of COPD
73.	Gene Mutations,Clinical Phenotype And Pedigree Analysis Of Inherited Coagulation Factor ? Deficiency:Analysis Of One Case
74.	Study Of Clinical Phenotype And LDL-R Gene Mutation In A Familial Hypercholesterolemia Family
75.	Effect Of Passive Smoking On Clinical Phenotype Of Patients With SLE
76.	Correlation Analysis Of HLA-DPB1 Gene And BTNL2 Gene Within MHC Region With Clinical Phenotype Of Psoriasis Vulgaris In The Chinese Han Population
77.	Correlation Analysis Of Genotype And Clinical Phenotype Of 21-hydroxylase Deficiency In Shanxi Province
78.	Study On The Correlation Between Methylation Level And Clinical Phenotype Of Peripheral Blood Mononuclear Cells In Patients With Systemic Lupus Erythematosus
79.	Detection And Clinical Phenotype Analysis Of Five Deafness Related Mitochondrial Candidate Genes In Patients With Nonsyndromic Hearing Loss
80.	Analysis Of Clinical Phenotype And Gene Mutation Characteristics Of Infants With Methylmalonic Acid
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