Clinical Phenotype - Globe Thesis

Keyword [Clinical Phenotype] Result: 21 - 40 \| Page: 2 of 9
21.	Association Between The Polymorphism Of XPD Lys751Gln And Clinical Phenotype And Response To Chemotherapy Of Non-Hodgkin's Lymphoma
22.	A Study On The Sero-epidemiology Of Hepatitis B In Children And The Hepatitis B Virus Genotype
23.	The Effect Of ApoE Genotype On Clinical Phenotype Of Hypoceruloplasminemia-related Movement Disorder
24.	Analysis Of The Relatoin Between Gene Mutation And Clinical Phenotype For Autosomal Recessive Families
25.	Clinical Features And Molecular Analysis Of Ten Patients With Wiskott-Aldrich Syndrome In China
26.	Study Of The Relationship Of SCN1A Genotype,Clinical Phenotype And The Effect Of Treatment In Severe Myoclonic Epilepsy In Infancy
27.	Relationship Between The Genotype And Clinical Pheotype In An Inherited Coagulation Factor VII Deficiency Family
28.	Study On The Relationship Of The ATP7B Gene Mutation And Clinical Phenotype In WD Patients
29.	Relationship Between The Genotype And Clinical Pheotype In An Inherited Coagulation Factor Vii Deficiency Family
30.	Type 2 Diabetes Yin Deficiency Clinical Phenotype And Serum No Correlation,
31.	Study Of Clinical Phenotype And Mechanism In Twenty-five Chinese Pedigrees With Glanzmann Thrombasthenia
32.	The Clinical Phenotype Research Of Myositis Specific Antibodies In Patients With Idiopathic Inflammatory Myopathies And Experimental Autoimmune Myositis In C57BL/6Mice
33.	Association Study Of HTR3A Gene Polymorphism With Major Depression And Clinical Phenotype
34.	Study On Factors Related To The Clinical Feature And Molecular Biology Of Hemorrhagic Moyamoya Disease
35.	The Study Of Clinical Phenotype, Growth Hormone Receptor (GHR) Exon 3 Polymorphism And Early Screening And Prevention Of Prader-Willi Syndrome
36.	Analysis Of The Genetic Characterization Of SSLP-D4Z4-4qA/qB-PLAM In Patients With FSAM And Its Association With Clinical Phenotype In Chinese Han Population
37.	Clinical Phenotype And Molecular Mechanism Of Hereditary Hemorrhagic Telangiectasia
38.	Study On The Defect Of SHOX Gene And Its Conserved Noncoding DNA Elements And The Relationships With Phenotypes And X-ray Of Idiopathic Short Stature
39.	Study Of Clinical Phenotype And Molecule Diagnostics Of Prader-Willi Syndrome
40.	Studies On Correlation Of Clinical Phenotype And RHO Gene Mutations In Non Syndromic Retinitis Pigmentosa
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