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Keyword [Whole Exome]
Result: 41 - 60 | Page: 3 of 10
41. Deep Sequencing Identifies Mutation Genes Related To TCCB And Validation Of The HECW1Mutation
42. A Pilot Study Of Human Whole-exome Sequencing On Gene Chip For Oral Cancer SNPS
43. Whole Exome Sequencing Identifying Genetic Etiology Of Congenital Scoliosis In Chinese Han Population
44. Whole Exome Sequencing Identifying Causative Gene In A Intracranial Aneurysm Pedigree
45. 1, Part I: Gene Pathogenic Female Reproductive Tract Abnormalities In Patients 2, Part II: Clinical Phenotype, Family History Research 98 Cases Of Chinese MRKH Syndrome And Psychological Functions
46. Research On The Cause Of Molecular Genetics MRKH Syndrome
47. All Exon Sequencing Applications In Neonatal Diabetes Research
48. Research On The Role And Mechanism Of SENP1and MLL3in Acute Leukemia
49. A Novel Mutation In The EMD Gene Caused Familial Dilated Cardiomyopathy
50. Exome Sequencing Identifies The Predisposing Gene For A NF1Pedigree Combined With CPT
51. Whole Exome Sequencing Identifying Frequent Alternations In Genes In Ovarian Endometriosis
52. Whole-Exome Sequencing In A Pedigree With Hereditary Non-Polyposis Colorectal Cancer (HNPCC)
53. Investigation Of Disease Causative Mutations In Multi Pedigrees With Mendelian Inherited Diseases
54. Detection Of Exome Copy Number Variation Based On Hidden Markov Model
55. Whole Exome Capture Sequencing Identifies Candidate Genes Related To Colon Cancer
56. The Screening Research Of Dopa-responsive Dystonia Gene Mutation In One Chinese Family
57. Genetic Analysis In Four Families With Early-onset Cognitive Dysfunction
58. The Collection And Gene Analysis Of Two Pedigrees With Suspected Hereditary Spastic Paraplegia From Guizhou
59. The Study Of Lung Cancer In XuanWei Revealed By Whole Genome And Exome Sequencing
60. Genetic Analysis Of A Family With Autosomal Dominant Nonsyndromic Hearing Loss
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