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Keyword [familial]
Result: 21 - 40 | Page: 2 of 10
21. Collection And Reservation Of Familial Adenomous Polyps Family Resources In Chinese And Analysis Of Its Clinical And Molecular Characteristics
22. Study On The Gene Variations And The Susceptibility Of Gastrointestinal Cancers
23. Clinical And Molecular Genetic Analysis Of Two Pedigree With Idiopathic Epileptic Syndromes
24. Infantile Progressive Intrahepatic Cholestasis And Mutations In Bile Salt Export Pump Gene
25. Gene Mapping And Identification For Osteoporosis And Benign Familial Adult Myoclonus Epilepsy
26. A Chinese Familial And Sporadic Cases With Congenital Fibrosis Of The Extraocular Muscles: Clinical And Molecular Genetic Study
27. Pedigree Investigation And Genetic Analysis Of Familial Atrial Septal Defect
28. Pedigree Investigation And Genetic Analysis Of Familial Cardiomyopathy And Conduction System Disease In Chinese
29. Study On The Aggregation Tendency Of Uterine Fibroids
30. Association Of Hepatitis B Virus Genotype, Gene Subtype And Basic Core Promoter Region / Pre - C Region Gene Mutation With Liver Cancer Family Aggregation In
31. Clinical Application Of Clinical Evaluation Of Clinical Evaluation Of Lymphatic Fibroids (LAM) And Birt-Hogg-Dubé (BHD) Syndrome
32. Genetic Susceptibility Of Children 's Still' S Disease And The Administration Of Pearl Monoclonal Antibody
33. Study On Adenomatous Polyposis Coli Gene Germline Mutation In Familial Adenomatous Polyposis
34. The Clinical Pathological Features And Carcinogenesis Of Familial Colorectal Cancer
35. The Genetic Trait And The Relationship Between Calpain10 Gene UCSNP43 And UCSNP44 Polymorphism And Diabetes In Familial Type 2 Diabetes Mellitus Of Uygur In Xinjiang.
36. Myotonic Dystrophy: Muscle Pathological, Electrophysiological, Myogenic Relation Factors' MRNA Expression And Familial Cases Review
37. Study On Targeted Correction Of Point Mutation In Low Density Lipoprotein Receptor Gene In Situ Of Chromosome And Regulatable Expression
38. Targeted Correction Of Point Mutations In Low Density Lipoprotein Receptor Gene Mediated By Modified Single Stranded Oligonucleotides In Mouse Liver In Vivo
39. Expresison Of E-cadherin And Adhesion Molecules Familial Members α-, β-, γ-, P120- Catenin In The Spinal Chordoma And Analysis Of The Correlating Prognosis
40. KCNJ5 Gly387Arg Mutation Responsible For Familial Long QT Syndrome
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