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Keyword [Pedigree]
Result: 1 - 20 | Page: 1 of 10
1. Clinical And Experimental Studies On The Constitutional Features And Their Implications In Tumorogenesis Among Population At High Risk Of Nasopharyngeal Carcinoma
2. The Study Of Relationship Between Two Frequent Polymorphisms In The Protein S Gene (PROS1) And Ischemic Stroke
3. The Study Of Pedigree And Initial Gene Location For Pathological Myopia
4. Structural And Genetic Analysis Of Human RH Gene
5. The Clinical Study On Tuberous Sclerosis Complex And Mutational Analysis Of TSC2 In Cases Of A Pedigree
6. Congenital Fibrosis Of The Extraocular Muscles In Chinese Families: Clinical Phenotype, Linkage Mapping, And Mutation Identification Of KIF21A
7. The Study On Mutation In Congenital Hypothyroidism
8. Population-based Epidemiology Survey And Pedigree-based Susceptibility Gene Study Of Rhegmatogenous Retinal Detachment
9. Mutation-function Analysis In The Lipoprotein Lipase Gene In Hypertriglyceridemic Members Of Type 2 Diabetic Pedigrees
10. Establish A Collecting System For Birth Defects Pedigrees And Mutation Analysis Of HOXD13 In A Chinese Pedigree With Synpolydactyly
11. Scan Of Susceptibility Gene For Familial Essential Hypertension(ESH) On Chromosome 1
12. The Association Between Coagulation System Activation And Risk Stratification Of Cerebral Infarction
13. Study On The Echocardiogram Features And The Genetic Laws Of Noncompaction Of The Ventricular Myocardium
14. The Clinical Characteristics, Pedigree Analysis And Mitochondrial DNA Mutation In Familial Dilated Cardiomyopathy
15. Clinical And Molecular Genetic Analysis Of Two Pedigree With Idiopathic Epileptic Syndromes
16. Candidate Genes Screen And Gene Mapping In Infantile Glaucoma Patients And Juvenile Glaucoma Pedigrees
17. Identification Of The Responsible Gene For A Dilated Cardiomyopathy Pedigree And Susceptibility Locus For Schizophrenia
18. Pedigree Investigation And Genetic Analysis Of Familial Atrial Septal Defect
19. Pedigree Investigation And Genetic Analysis Of Familial Cardiomyopathy And Conduction System Disease In Chinese
20. Study On Sample Storage And Smad2 Gene Mutation In A Han Chinese Keloid Pedigree
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