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Keyword [Families]
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1. The Clinical Aspects And Molecule Mechanisms Of Congenital Coagulation Factor V Deficiency: Studies Of Two Families
2. Mapping Of Pathogenic Gene In Three DGI-Ⅱ Families
3. The Significance Of Expression Of Vascular Endothelial Cell Growth Factor Families And Their Receptors In Breast Carcinoma And Being A Target For Antiangiogenesis Therapy
4. Mutation Patterns In MMR Genes And Clinical Phenotypes Of HNPCC Families In The Northern Chinese Population
5. Gene Mapping And Mutation Detection In Families With Hereditary Spastic Paraplegia
6. Genetic Mapping And Mutation Analysis In Chinese Families With Congenitial Cataract
7. Congenital Fibrosis Of The Extraocular Muscles In Chinese Families: Clinical Phenotype, Linkage Mapping, And Mutation Identification Of KIF21A
8. Expression Characteristic Of Three Hsps Gene Families During Normal Organs Development And During Short-limb And Cleft Palate Development In ICR Mouse
9. Gene Mapping And Analysis Of Candidate Genes In Two Chinese Families With Retinitis Pigmentosa
10. The Significance Of Expression Of Vascular Endothelial Cell Growth Factor Families And Their Receptors In Non-small Cell Lung Carcinoma And Being A Target For Gene Therapy
11. The Clinical Characterization Of HNPCC Families From Northern Chinese Population And The Role Of HMLH3 And HEXO1 Germline Mutation In HNPCC
12. Families Investigation, Genetic Analysis And Molecular Mechanism On Cherubism
13. Characterization Of Genotype-phenotype And Clinico-pathological Features In Chinese Hereditary Nonpolyposis Colorectal Cancer Families
14. Mapping And Identification Of The Responsible Gene For Cataracts In Chinese Families
15. Mapping, Candidate Cloning Of A Novel Disease Gene For BFIC And The Mutation Analysis Of KCNQ3 Gene In BFNC Families
16. Mapping The Disease Gene In SCA Families And The Frequency Distribution Analysis Of Different Subtypes Of SCA In Hans Of China
17. Study Of Screening Hereditary Nonpolyposis Colorectal Cancer Families Based On MRNA Sequencing
18. Different Attitudes Of Patients, Families, Oncology Clinicians, And Oncology Nurses Toward Truth Telling Of Cancer Diagnosis
19. Mutational Analyses Of The Cathepsin C Gene (CTSC) In The Han Nationality Families With Papillon Lefèvre Syndrome
20. Analysis Of Clinical Features And Study Of Responsible Genes For The Chinese Retinitis Pigmentosa And Usher Syndrome Families
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