Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2191 Sort by:
  • Von Willebrand Disease, Type 1
    OMIM # 193400
    VWD1, Von Willebrand Disease, Type I, VWD, Type 1,
  • Von Willebrand Disease, Type 2
    OMIM # 613554
    VWD2, Von Willebrand Disease, Type II, VWD, Type 2,
  • BRCA1-Interacting Protein
    OMIM # 605882
    BRIP1, BRCA1-Associated C-Terminal Helicase 1, BACH1, Deletions of Guanine-Rich DNA, C. Elegans, Homolog of, DOG1, Homolog of, FANCJ Gene, FANCJ,
  • Centrosome Spindle Pole-Associated Protein 1
    OMIM # 611654
    CSPP1, CSPP,
  • Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
    OMIM # 610199
    NDH, NDH Syndrome,
  • Doublecortin-Like Kinase 2
    OMIM # 613166
    DCLK2, DCK2, CAMK-Like CREB Regulatory Kinase 2, CLICK2, CL2,
  • Eukaryotic Translation Initiation Factor 4A, Isoform 3
    OMIM # 608546
    EIF4A3, DEAD/H Box 48, DDX48, NUK34, Nuclear Matrix Protein 265, NMP265, KIAA0111,
  • FANCC Gene
    OMIM # 613899
    FANCC, FAC, FACC,
  • GLIS Family Zinc Finger Protein 3
    OMIM # 610192
    GLIS3, GLI-Similar Protein 3, Zinc Finger Protein 515, ZNF515,
  • Integrin, Alpha-1
    OMIM # 192968
    ITGA1, Very Late Activation Protein 1, VLA1, CD49 Antigen-Like Family Member A, CD49a,
  1. <<
  2. ...
  3. 11
  4. 12
  5. 13
  6. 14
  7. 15
  8. 16
  9. 17
  10. 18
  11. 19
  12. 20
  13. 21
  14. 22
  15. ...
  16. >>