Pedigrees - Globe Thesis

Keyword [Pedigrees] Result: 61 - 80 \| Page: 4 of 5
61.	Study On The Clinical Phenotype And Mechanism In Two Chinese Pedigrees With Von Willebrand Disease
62.	Research On Genetics Of Familial Diabetes In Yunnan Han Population DNA3243,3316,3394,3714 Mitochondrial Mutation Sites
63.	Detection Of The STS Gene And Flanking Sequences Of Two Chinese Pedigrees With X-linked Ichthyosis
64.	Investigation Of Disease Causative Mutations In Multi Pedigrees With Mendelian Inherited Diseases
65.	Analyzing MEN2A By Whole Genome Sequencing, And Gene Mutation Analysis And Prenatal DNA Diagnosis Of6EPPK Pedigrees
66.	Mutation Detection In Coding Regions Of NLGN4 Gene In Mental Retardation Patients And Pedigrees Of Qinba Mountain Area
67.	The Functional Characterization Study Of SLC12A3 Gene Mutation Causing Gitelman Syndrome In Two Pedigrees
68.	The Collection And Gene Analysis Of Two Pedigrees With Suspected Hereditary Spastic Paraplegia From Guizhou
69.	SLC4A1 Matations In Chinese Pedigrees With Hereditary Spherocytosis
70.	Investigation In Abnormal Metabolism Of The Patients Of Familial Nonalcoholic Fatty Liver Disease And Their First-Degree Relatives
71.	Study Of The Molecular Mechanism In Two X-linked Hypophosphatemic Rickets Pedigrees
72.	A Study On The Relationship Between The Single Nucleotide Polymorphism Of TSPAN8 Gene And Susceptibility Of Hepatocellular Carcinoma Pedigrees In Fusui County Of Guangxi Zhuang Autonomous Region
73.	Generalized Disequilibrium Test For Association In Qualitative Traits Incorporating Imprinting Effects And Maternal Effect Based On Extended Pedigrees
74.	Study Of Genetic Variability Of Hepatocyte Nuclear Factor-1? Gene In Three Chinese Pedigrees With Early-onset Diabetes
75.	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
76.	Investigation And Genetic Analysis Of Chinese Han Graves' Disease Multiplex Pedigrees
77.	Whole Exome Sequencing Identifies Pathogenic Genes Of Two Mendelian Genetic Disease Pedigrees And Function Characterization
78.	Identification Of Molecular Etiology In Pedigrees With Inherited Hearing Loss And Study Of Noninvasive Prenatal Testing Of Hearing Loss
79.	Serum Proteomics Screening And Target Protein Biomarkers Verifying On Uyghur MODY Pedigrees
80.	Identification And Characterzations Of Novel ADRB3 Mutations In Chinese Familial Gout Pedigrees
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