Font Size: a A A
Keyword [epidermolysis]
Result: 1 - 20 | Page: 1 of 2
1. Mutations Of COL7Al Gene Of Dystrophic Epidermolysis Bullosa Pruriginosa
2. Dystrophic Epidermolysis Bullosa: Analysis Of Clinical And Genetic Features And Study On The Structure Deficiency Of Basement Membrane Zone
3. Laboratory Diagnoses Of Epidermolysis Bullosa Acquisita
4. Study On Gene Mutation Of Two Dystrophic Epidermolysis Bullosa Pedigrees
5. Dominant Dystrophic Epidermolysis Bullosa: Mutation Analysis
6. Mutation Analysis Of COL7A1 Gene In Two Chinese Families With Dystrophic Epidermolysis Bullosa Pruriginosa
7. The Report Of One Clan With Dystrophic Epidermolysis Bullosa Dominant
8. Restoration Of Recombinant Human Type VII Collagen And Correction Of The Disease Phenotype In A Murine Model Of Dystrophic Epidermolysis Bullosa
9. Mutation Analysis Of The Keratin 5 And 14 Genes In Chinese Patients With Epidermolysis Bullosa Simplex
10. COL7A1 Gene Mutation Analysis In A Family With Pasini Epidermolysis Bullosa
11. Col7a1 Gene Mutation Analysis In A Family With Pasini Epidermolysis Bullosa
12. Eye Fissure Narrow Syndrome, Atopic Dermatitis And Other Skin Diseases, Gene Mutation Studies
13. The Genotype-phenotype Correlation In Epidermolysis Bullosa
14. Epidermolytic Palmoplantar Keratoderma:Genotype-Phenotype Correlation, Prenatal Genetics Diagnosis And Knock-in Mouse Model
15. Genotype-phenotype Correlation In One Epidermolytic Palmoplantar Keratoderma And Two Pachyonychia Congenital Type â… Pedigrees
16. Mutation Analysis Of The Genes In Chinese Patients With Epidermolysis Bullosa Simplex And Dominant Dystrophic Epidermolysis Bullosa
17. The Effect Of G31P, CXCR1/2Antagonist, On Lesional Skin Of Epidermolysis Bullosa Acquisita
18. Dystrophic Epidermolysis Bullosa Syndrome
19. Research On Gene Mutations In Patients With Epidermolysis Bullosa Simplex With Mottled Pigmentation In Ningxia
20. Analyzing MEN2A By Whole Genome Sequencing, And Gene Mutation Analysis And Prenatal DNA Diagnosis Of6EPPK Pedigrees
  <<First  <Prev  Next>  Last>>  Jump to