Heterozygous mutation - Globe Thesis

Keyword [Heterozygous mutation] Result: 1 - 20 \| Page: 1 of 2
1.	Study Of Activation Of BTAK Expression In Primary Ovarian Surface Epithelial Cells Carrying Heterozygous BRCA Mutation And Tumorigenesis Of Ovarian Carcinoma
2.	Signaling Role Of Prokineticin2/Prokineticin Receptor2in Female Reproduction System
3.	Analysis Of TGFBI Gene Mutation In A Chinese Family With Lattice Corneal Dystrophy I
4.	A New Compound Heterozygous Mutation In CYP17A1 Gene Causes 17Î±-hydroxylase Deficiency And Pedigree Study
5.	Molecular Genetics Of A Chinese Family With Avellino Corneal Dystrophy
6.	Study Of Phenotype And Genetic Characteristics Of Mada Pedigree
7.	Mutation Analysis Of DYSF Gene In A Chinese Family With Dysferlinopathy
8.	Analysis Of The Mutations Of APC Gene In A Family With Familial Adenomatous Polyposis
9.	Screening And Analysis Of A Pathogenic Gene In A Myasthenia Gravis Family
10.	Mutation Screening In Families With Two Rare Diseases By Candidate Gene Approach
11.	Molecular Study Of MiR-184-mediated Suppression Of Retinoblastoma And The Tujia Congenital Aniridia Family PAX6 Mutation Loci Analysis
12.	Analysis Of A Family With MODY Caused By A Mutation In The INS Gene
13.	Clinical Analysis Of 36 Patients With Gitelman Syndrome And 1 Patient With SLC12A3/KCNJ1 Double Heterozygous Mutation
14.	The Research On Second-Generation Sequencing And Mutation Analysis Of 5 Patients With Gitelman’s Syndrome Caused By Complex Heterozygous Mutation Of SLC12A3 Gene
15.	The Clinical Features Of Patients With Dominant Cerebral Small Vessel Disease And Heterozygous HTRA1 Mutation
16.	The Pathogenic Mechanism Studies And The Genotype-Phenotype Correlation Of MYH3 Associated Congenital Scoliosis
17.	A Novel Compound Heterozygous Mutation In ABCA3 Gene In A Child With Interstitial Lung Disease
18.	Analysis Of Clinical Features And Genotype-phenotype Correlations In Patients With Heterozygous HTRA1-related Cerebral Small Vessel Disease
19.	Study On The Mutation Spectrum And Pathogenic Mechanism Of ALPK3 Gene In Congenital Scoliosi
20.	Application Of Carrier Screening Of Monogenic Disease Based On Capillary Electrophoresis Platform
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