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Keyword [congenital]
Result: 21 - 40 | Page: 2 of 10
21. The Metabolic Alteration Of Bile Acids In The Bile And Serum In Child With Congenital Biliary Dilation
22. Clinical Applications Of Transpulmonary Thermodilution Technique In Children With Congenital Heart Disease
23. Methodological Study Of Transthoracic Real-time Three-dimensional Echocardiography And Its Application In The Evaluation Of Congenital Heart Diseases In Children
24. Strategy For Prenatal Diagnosis Of Congenital Heart Disease And Evaluation Of Its Effectiveness
25. The Treatment By Dialectics And Study Of The Development Dislocation Of The Hip
26. The Study On Pathogenic Gene Of Hereditary Progressive Cortical Cataract
27. Ultrastructure Analysis And Linkage Mapping Of The Family With Congenital Cataract
28. 1,TBX5 Gene And Cardiac Development 2,Analysis Of SNP And Haplotype In HOXC Gene Cluster Within Susceptible Region 12q13 Of Simple Congenital Heart Disease
29. Mapping And Postional Cloning The Causative Genes In Chinese Pedigrees With Non-syndromic Hereditary Hearing Impairment
30. Nitric Oxide As A Method To Screen And Treat Patients And Affect Vascular Smooth Muscle Cell Apoptosis And Expression Of Apoptosis-Specific Genes In Congenital Heart Disease, Left To Right Shunt And Pulmonary Hypertension Before Operation
31. Evaluation Of Pulmonary Hypertension (PH) And Right Ventricular Function In Patients With Congenital Heart Disease And PH Using Radionuclide Scintigraphy
32. Research For Associated Gene Of Congenital Heart Disease
33. The Comparative Study Between Diagnostic Imaging And Pathology In Congenital Heart Defects Associated With Severe Pulmonary Hypertension In Young Children
34. The Clinic Epidemiologic Survey For Congenital Microtia
35. Study Of CFTR Gene Mutations And Testicular Ultrastructure And ICSI Of Congenital Obstructive Azoospermia
36. Clinical Studies Of The Extracardiac Conduit Total Cavopulmonary Connction
37. Experimental And Clinical Studies Of Severe Complex Congenital Heart Disease With Decreased Pulmonary Blood Flow
38. Identification Of The Mutant Gene Responsible For The CSNB Rat
39. Study On The Clinical Characteristics And The Genetic Mutations Of 17α-hydroxylase/17, 20-lyase Deficiency
40. Transcatheter Closure Of Secundum Septal Defect By Amplatzer Occluder And Realated Study
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