Missense mutation - Globe Thesis

Keyword [Missense mutation] Result: 41 - 57 \| Page: 3 of 3
41.	Mutation Analysis Of PMM2 Gene In Congenital Disorders Of Glycosylation And Literature Review
42.	The Pathogenic Gene Study Of A Family With Hashimoto's Thyroiditis And The Association Analysis Of SNP Rs12532, Rs870142 And The Risk Of Congenital Heart Disease In Tibetans
43.	A Molecular Mechanism Study On The Influence Of Genetic Factors Of The GRN Gene Mutation And Metabolic Factors Of Type 2 Diabetes Mellitus On Parkinson's Syndrome
44.	Molecular Genetic Mechanism Research Of Liddle Syndrome Caused By A Novel SCNN1B Missense Mutation
45.	The Pathogenic Mechanism Studies And The Genotype-Phenotype Correlation Of MYH3 Associated Congenital Scoliosis
46.	A Natural DNMT1 Missense Mutation Elevates Fetal Hemoglobin Via Epigenetic De-Repression Of The ?-Globin Gene In ?-Thalassemia
47.	Three-dimensional Bioprinting In Constructing Tumor Microenvironment Model For Hepatocellular Carcinoma
48.	Screening Of Cancer Associated Gene Mutations And Its Clinical Significance In Oral Squamous Cell Carcinoma
49.	Identification And Mechanism Investigation Of Pathogenic Gene Mutation In VHL Syndrome
50.	Study On The Mechanism Of Acephalic Spermatozoa Syndrome Caused By A Novel Mutation In PMFBP1
51.	Pathogenicity Study Of Limb-girdle Muscular Dystrophy Type 2Q Caused By Plec Gene Novel Mutations
52.	The Molecular Mechanism Of MYH13 Gene Mutation With Aniridia And Study On CMY2Q Mouse Model
53.	A Novel P.G1344E Mutation In FBN1 Is Associated With Ectopia Lentis
54.	Pathogenicity Analysis Of A Severe Nonsyndromic Tooth Agenesis Case
55.	Screening And Analysis Of Genetic Susceptibility Genes In A Family With Progressive Atrioventricular Block In Hainan
56.	A Pedigree Study Of Congenital Sideroblastic Anemia Caused By NDUFB11 Gene Mutation
57.	The Role Of Rare Variants In The CTSD Gene In Neuronal Ceroid Lipofuscinosis Type 10
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