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Keyword [Mutation identification]
Result: 1 - 15 | Page: 1 of 1
1. Congenital Fibrosis Of The Extraocular Muscles In Chinese Families: Clinical Phenotype, Linkage Mapping, And Mutation Identification Of KIF21A
2. Mutation Identification And Functional Analysis Of ADAR, The Disease Gene For Dyschromatosis Symmetrica Hereditaria
3. Molecular Genetics Of Limb Malformations: Mutation Identification In HOXD13, TNNI2 And TPM2
4. Congenital Generalized Hypertrichosis Terminalis: Genetic Mapping And Pathogenic Mutation Identification
5. Mutation Identification In A Han Chinese Kindred With Hereditary Multiple Exostosis And Three Acne Inversa Families
6. Mutation Identification Of Pathogenic Gene For Two Families With Limb Malformation
7. Mutation Identification And Functional Analysis Of Disease Gene In A Family With Congenital Cataract
8. Identification Of The Causative Mutations For Two Families With Monogenic Diseases
9. Mutation Identification And Functional Analysis Of Disease Gene In A Family With Mendelian Susceptibility To Mycobacterial Disease
10. Mutation Identification And Functional Analysis Of Disease Gene In Three Chinese Families With Mendelian Susceptibility To Mycobacterial Disease
11. A Novel PAX9 Mutation Identification And Functional Verification Of A Patient With Congenital Non-syndromic Hypodontia
12. The Algorithms And Models For Cancer Driver Mutation Identification
13. Genetic Study Of Congenital Painless And Anhidrosis
14. Mutation Identification And Mechanism Research Of Pathogenic Genes In Abnormal Zone Pellucida Disease Family
15. Mutation Identification Of Disease Gene In Pedigrees With Oocyte Maturation Arrest And Pathogenic Mechanism Analysis Of PATL2 Gene Mutations
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