Causative gene - Globe Thesis

Keyword [Causative gene] Result: 21 - 40 \| Page: 2 of 3
21.	Identification Of The Causative Gene Of A Nonsyndromic Retinitis Pigmentosa Pedigree
22.	Identification Of A Causative Gene In A High Myopia Family
23.	Identification And Function Analysis Of Hereditary Spastic Paraplegia Causative Gene SLC33A1 Mutation Site C.339T>G (p.Ser113Arg)
24.	Study On The Molecular Genetic Between Hypertrophic Cardiomyopathy And FKBP12.6
25.	Localization Of A Chinese Familial Cortical Myoclonic Tremor With Epilepsy Pedigree
26.	A Pedigree Study Of Frontotemporal Dementia And Retrospective Analysis Of The Clinical Features Of Frontotemporal Dementia
27.	Whole Exome Sequencing Searchs For The Causative Gene Of Familial Progressive Hyper- And Hypopigmentation In One Chinese Family
28.	Identification Of PMVK As A New Causative Gene For Disseminated SuperficialPorokeratosis
29.	The Functional Study Of Cenani-Lenz Syndactyly Syndrome Causative Gene LRP4 In Limb And Kidney Development
30.	The Study On The Causative Gene Of Common Spinocerebellar Ataxia Subtypes In Guangxi Zhuang Normal Population
31.	Localization Of A Familial Cortical Myoclonic Tremor With Epilepsy Pedigree
32.	Whole Exome Sequencing Identifies The Causative Gene Mutation In A Chinese Family With Hereditary Spastic Paraplegias
33.	Identifying The Causative Gene Of An Olmsted Syndrome Kindred By Whole Exome Sequencing,and KRT9 Gene Mutation Analysis And Prenatal DNA Diagnosis Of Four Epidermolytic Palmoplantar Keratoderma Pedigrees
34.	Identification Of The Causative Genes For Three Chinese Families With Autosomal Dominant Retinitis Pigmentosa
35.	Identification Of Causative Gene Mutation And Pathological Mechanism In A Bardet-biedl Syndrome Family
36.	Verification Of The Causative Gene In PADMAL Variant And Pathological Mechanisms Of SMEK1 In Neuropathy
37.	A New Causative Gene ARMC5 Mutation Indentified By Whole-exome Sequencing In Primary Bilateral Macronodular Adrenal Hyperplasia
38.	Preliminary Identification Of Causative Gene For Tuberous Sclerosis Complex
39.	Whole Exome Sequencing Identifying Causative Gene In A Migraine Without Aura Pedigree
40.	Identification And Functional Analysis Of Causative Gene In An Autosomal Recessive Family With Lipid Deposition And Joint Contracture
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