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Keyword [LINKAGE analysis]
Result: 41 - 60 | Page: 3 of 10
41. Identification Of Polymorphism Of INOS Gene Associated With Essential Hypertension
42. Preliminary Linkage Analysis Of Keloid Susceptibility Loci And Polymorphisms Of Correlation Genes In Chinese Han Population
43. Detection Of Interaction Between Wild Type ADAR1 Protein And Its R916W Mutant Using Yeast And Mammalian Two Hybrid Systems And Gene Locus And Mutation Screening In Marie Unna Hereditary Hypotrichosis
44. RP33, A Novel Locus Of Autosomal Dominant Retinitis Pigmentosa; And A Complete Mutation Screening Of PRPF31 Gene In RP11 Linked Family
45. A Chinese Familial And Sporadic Cases With Congenital Fibrosis Of The Extraocular Muscles: Clinical And Molecular Genetic Study
46. Identification Of The Responsible Gene For A Dilated Cardiomyopathy Pedigree And Susceptibility Locus For Schizophrenia
47. Fine Mapping Psoriasis Susceptibility Genes In Chinese Han Population
48. Refine Mapping Study Of Susceptibility Genes For Chinese Hans Vitiligo
49. Study On Fas Gene Mutation And Location Of Predisposing Gene On Chromosomes 2q23 For Chinese Keloid Pedigrees
50. 1. Linkage Analysis And Mutation Screening In Triphalangeal Thumb-Associated Limb Malformations 2. Generation Of Fgfr3+/P244R Mouse Chimera And Phenotype Analysis Of Fgfr2+/P253R Mouse Model
51. The Positional Cloning Of A Complex Nervous System Disease From A Chinese Pedigree
52. Genetic Analysis Of Non-syndromic Hearing Loss And Waardenburg Syndrome
53. Gene Mapping And Analysis Of Candidate Genes In Three Chinese Families With Congenital Cataract
54. Ultrastructural Study Of The Extraocular Muscles And Analysis Of Gene Mutation In Congenital Nystagmus
55. Mapping The Disease-causative Gene For Pedigree Li With Primary Open Angle Glaucoma In Zhongxian, Chongqing
56. The Clinic And Basic Research On Leber Eye Disease And Congenital Cataract
57. Molecular Cytogenetics Study Of Three Kinds Of Hereditary Neurogenetic Diseases
58. Mapping And Positional Cloning The Causative Genes In Chinese Pedigrees With Non-syndromic Hereditary Hearing Impairment
59. Congenital Generalized Hypertrichosis Terminalis: Genetic Mapping And Pathogenic Mutation Identification
60. The Molecular Genetics Research Of Two Retinitis Pigmentosa Pedigrees
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