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Keyword [Pedigrees]
Result: 81 - 99 | Page: 5 of 5
81. Clinical Observation Of Three Fibronectin Nephropathy Pedigrees And Pathogenicity Analysis Of FN1 Gene Mutation
82. The Clinical,Electrophysiological And Genetic Analysis On Three Pedigrees Of Hereditary Neuropathy With Liability To Pressure Palsies
83. A Study On The Reationship Between The Single Nucleotide Polymorphism Of GHR Gene And Genetic Susceptibility Of Hepatocellular Carcinoma Pedigrees In Guangxi Zhuang Autonomous Reg
84. Mapping And Identification Of The Causative Genes In Three Chinese Pedigrees With Autosomal Dominant Hereditary Hearing Loss
85. Screening Of Pedigrees Of Primary Biliary Cholangitis And Exploration Of Rare Mutations By Whole Exome Sequencing
86. Characteristics And Follow-Up Of Pedigrees With Gitelman Syndrome
87. Study Of Prevalence And Characteristics In Gallstone Pedigrees
88. Screening And Diagnosis Of Fabry Disease And Analysis Of Clinical And Genetic Characteristics In Pedigrees
89. Screening And Functional Characterization Of The WFS1 Gene Mutations Identified From Wolfram Syndrome Pedigrees And Bioinformatic Analysis Of WFS1 Gene
90. Research On Gene And Molecular Mechanism In Three Pedigrees With MYH9-related Disorder
91. Research On Gene And Molecular Mechanism In Two Pedigrees With Wiskott-Aldrich Syndrome
92. Analysis of extended pedigrees for localizing of genes in neuropsychiatric disorders
93. Analysis of extended pedigrees ascertained for asthma
94. Family cancer history and pedigrees as a public health intervention for promoting health and preventing prostate cancer in African-Americans
95. The Study Of The Clinical Characteristics And RET Proto-oncogene Mutation In 2 Pedigrees Of Multiple Endocrine Neoplasia Type 2A
96. Genetic Mapping And Gene Diagnosis For Inherited Deafness Pedigrees
97. Clinical And Genetic Research Of 150 Pedigrees With Hereditary Spastic Paraparesis
98. The Study On Whole Exome Sequencing Of Deafness Gene In Pedigrees Of Non-syndromic Hearing Loss In Guangxi Region
99. Mutation Identification Of Disease Gene In Pedigrees With Oocyte Maturation Arrest And Pathogenic Mechanism Analysis Of PATL2 Gene Mutations
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