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Keyword [whole-exome sequencing]
Result: 41 - 60 | Page: 3 of 10
41. Research On The Cause Of Molecular Genetics MRKH Syndrome
42. All Exon Sequencing Applications In Neonatal Diabetes Research
43. Research On The Role And Mechanism Of SENP1and MLL3in Acute Leukemia
44. A Novel Mutation In The EMD Gene Caused Familial Dilated Cardiomyopathy
45. Exome Sequencing Identifies The Predisposing Gene For A NF1Pedigree Combined With CPT
46. Whole Exome Sequencing Identifying Frequent Alternations In Genes In Ovarian Endometriosis
47. Whole-Exome Sequencing In A Pedigree With Hereditary Non-Polyposis Colorectal Cancer (HNPCC)
48. Detection Of Exome Copy Number Variation Based On Hidden Markov Model
49. The Screening Research Of Dopa-responsive Dystonia Gene Mutation In One Chinese Family
50. Genetic Analysis In Four Families With Early-onset Cognitive Dysfunction
51. The Collection And Gene Analysis Of Two Pedigrees With Suspected Hereditary Spastic Paraplegia From Guizhou
52. The Study Of Lung Cancer In XuanWei Revealed By Whole Genome And Exome Sequencing
53. Genetic Analysis Of A Family With Autosomal Dominant Nonsyndromic Hearing Loss
54. The Role Of FUT6 In TGF-β1 Induced Epithelial-Mesenchymal Transition Of Renal Tubular Epithelial Cells
55. Identification Of A Novel Mutation In The SAG Gene In A Chinese Family With Autosomal Dominant Retinitis Pigmentosa
56. A Clinical And Genetic Research Of A Rare Pontocerebellar Hypoplasia Family
57. Whole Exome Sequencing Searchs For The Causative Gene Of Familial Progressive Hyper- And Hypopigmentation In One Chinese Family
58. Exploring The Genetic Susceptibility To Penicillium Marneffei Infection By Whole Exome Sequencing
59. 1 Analysis Of ZRS Mutations In Two Families With Triphalangeal Thumbs And Preaxial Polydactyly 2.The Preliminary Genetic Study Of Familial Nonmedullary Thyroid Cancer
60. Identification Of Susceptibility Genes In Kawasaki Disease Using Whole Exome Sequencing
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