Hereditary - Globe Thesis

Keyword [Hereditary] Result: 41 - 60 \| Page: 3 of 10
41.	Identification Of A Novel Locus For A New Clinical Variant Of Hereditary Alopecia In A Large Chinese Family By A Genome-Wide Scan
42.	Molecular Genetic Analysis Of Hereditary Eye Diseases
43.	A Case-control Study On The Association Between Genetic Polymorphisms Of DNA Rapair And Hepatic Cell Cancer Susceptibility
44.	The Clinical Values And Molecular Biological Features Of Screening The Chinese Hereditary Nonpolyposis Colorectal Cancer With NCCN Recommended Protocol
45.	Study On The Related Gene Of EOPD: MAO-B And COMT
46.	Study On The Germline Mutation Of HMSH6 Gene, Large Genomic Deletions Of Mismatch Repair Genes And The Methylation Of The HMLH1 Promoter In Hereditary Nonpolyposis Colorectal Cancer Families
47.	Molecular Cytogenetics Study Of Three Kinds Of Hereditary Neurogenetic Diseases
48.	Mapping And Positional Cloning The Causative Genes In Chinese Pedigrees With Non-syndromic Hereditary Hearing Impairment
49.	Characteristics Of Mutation Of Disease-causing Genes In Chinese Patients Diagnosed As Hereditary Spastic Paraplegia And Its Relation To Clinical Phenotype
50.	Molecular Genetic And Clinical Study Of Chinese Leber Hereditary Optic Neuropathy
51.	Study On The Thrombophilia Factors Of Venous Thromboembolism Patients And On Relationship Between Factors And TCM Syndrome Types
52.	The Research Of Hereditary Breast Cancer Susceptibility Genes Of Hunan Population In China With Familial Breast Cancer Or Early-onset Breast Cancer
53.	Molecular Genetic Analysis Of Chinese Hearing Loss Population
54.	Analysis Of Multiple Gene Polymorphisms For Molecular Prediction Of HBV-Related Cirrhosis Risk
55.	Study On The Germline Mutation Of HPMS2 Gene In Hereditary Bonpolyposis Colorectal Cancer Families And Screening Significance Of BRAF/KRAS In HNPCC
56.	The Study On The Relationship Between The Genetic Polymorphisms And MRNA Expression Of Arsenic Metabolic Genes And The Susceptibility Of Arsenism And Arsenic Methylation
57.	Mutation Identification In A Han Chinese Kindred With Hereditary Multiple Exostosis And Three Acne Inversa Families
58.	Study Of Molecular Mechanism Of Autosomal Dominant Nonsyndromic Hereditary Hearing Loss And Pfeiffer Syndrome
59.	Study Of Molecular Mechanism Of Non-syndromic Hereditary Hearing Loss
60.	Research On BRCA1/2 Mutations And Its Clinical Importance In Ovarian Cancer Patients From Families At Risk Of Hereditary Ovarian Cancer And Patients With Sporadic Ovarian Cancer
<<First <Prev Next> Last>> Jump to