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Showing below up to 100 results in range #201 to #300.

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  1. 2,5-Dimethylfuran‏‎ (1 revision)
  2. 3-hydroxy-3-methylglutaryl-CoA lyase deficiency‏‎ (1 revision)
  3. 8-cell stage‏‎ (1 revision)
  4. 9q34 deletion syndrome‏‎ (1 revision)
  5. 8-Aminoquinoline‏‎ (1 revision)
  6. 2-Acetylaminofluorene‏‎ (1 revision)
  7. 2-Aminoethoxydiphenyl borate‏‎ (1 revision)
  8. 2-Aminomuconic acid‏‎ (1 revision)
  9. A2ML1‏‎ (1 revision)
  10. ACACA‏‎ (1 revision)
  11. A-box 1 of insulin gene‏‎ (1 revision)
  12. AAAS (gene)‏‎ (1 revision)
  13. 2-Bromopropane‏‎ (1 revision)
  14. 2-Butyl-3-(p-tolyl)quinuclidine‏‎ (1 revision)
  15. 2-Chlorophenol‏‎ (1 revision)
  16. 2-Ethylhexanol‏‎ (1 revision)
  17. AADACL4‏‎ (1 revision)
  18. 2-Hydroxyglutaricaciduria‏‎ (1 revision)
  19. 2-Iodoxybenzoic acid‏‎ (1 revision)
  20. 2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene‏‎ (1 revision)
  21. 2-Me-DET‏‎ (1 revision)
  22. 2-Methyl-2-nitrosopropane‏‎ (1 revision)
  23. 2-Methyl-3,3-diphenyl-3-propanolamine‏‎ (1 revision)
  24. 2-Methyl-4-Chlorophenoxyacetic Acid‏‎ (1 revision)
  25. 2-Methylbutyryl-CoA‏‎ (1 revision)
  26. 2-Methylbutyryl-CoA dehydrogenase deficiency‏‎ (1 revision)
  27. 2-Nitropropane‏‎ (1 revision)
  28. 2-Nonenal‏‎ (1 revision)
  29. AARS2‏‎ (1 revision)
  30. 2-Phenylphenol‏‎ (1 revision)
  31. 2-Pyridone‏‎ (1 revision)
  32. 2-Pyrone‏‎ (1 revision)
  33. 2-chloroethanol‏‎ (1 revision)
  34. 2-hydroxyphytanoyl-CoA lyase‏‎ (1 revision)
  35. ABCA10‏‎ (1 revision)
  36. 2-propanoyl-3-(4-isopropylphenyl)-tropane‏‎ (1 revision)
  37. ABCA9‏‎ (1 revision)
  38. ABCC12‏‎ (1 revision)
  39. ABCB11‏‎ (1 revision)
  40. 2007 WikiDoc Foundation Scholars‏‎ (1 revision)
  41. 4,5-MDO-DMT‏‎ (1 revision)
  42. 5-alpha-reductase deficiency case study one‏‎ (1 revision)
  43. 4-Hydroxytestosterone‏‎ (1 revision)
  44. ABCC9‏‎ (1 revision)
  45. 2018 ACC/AHA/HRS Guideline on the Evaluation and Management of Patients With Bradycardia and Cardiac Conduction Delay‏‎ (1 revision)
  46. 4-MTA‏‎ (1 revision)
  47. 3c syndrome‏‎ (1 revision)
  48. 21-Hydroxylase Deficiency (patient information)‏‎ (1 revision)
  49. ABRA (gene)‏‎ (1 revision)
  50. ABI gene family member 3‏‎ (1 revision)
  51. 4-MeO-MiPT‏‎ (1 revision)
  52. 5'-phosphoribosyl-5-aminoimidazole‏‎ (1 revision)
  53. ACAA1‏‎ (1 revision)
  54. Ф29 phage‏‎ (1 revision)
  55. 5' flanking region‏‎ (1 revision)
  56. 5,6-MDO-DiPT‏‎ (1 revision)
  57. 5-Formamidoimidazole-4-carboxamide ribotide‏‎ (1 revision)
  58. 5,6-MeO-MiPT‏‎ (1 revision)
  59. 4-Methylbenzylidene camphor‏‎ (1 revision)
  60. 5-Hydroxyindoleacetic acid‏‎ (1 revision)
  61. 4-Nitroaniline‏‎ (1 revision)
  62. 5-alpha-reductase deficiency primary prevention‏‎ (1 revision)
  63. 4-Methylthioamphetamine‏‎ (1 revision)
  64. 5-MeO-DET‏‎ (1 revision)
  65. 5-MeO-DALT‏‎ (1 revision)
  66. 5-alpha-reductase deficiency cost-effectiveness of therapy‏‎ (1 revision)
  67. 4-Chloroindole-3-acetic acid‏‎ (1 revision)
  68. 5-MeO-pyr-T‏‎ (1 revision)
  69. 4-Oxalocrotonate tautomerase‏‎ (1 revision)
  70. 40S‏‎ (1 revision)
  71. 5-Methoxy-diisopropyltryptamine‏‎ (1 revision)
  72. 4-Dimethylaminophenol‏‎ (1 revision)
  73. 5-Methylindole‏‎ (1 revision)
  74. 5-Methylcytosine‏‎ (1 revision)
  75. 5-bromouracil‏‎ (1 revision)
  76. 5-Methyltetrahydrofolate‏‎ (1 revision)
  77. 60S ribosomal protein L28‏‎ (1 revision)
  78. 60S ribosomal protein L17‏‎ (1 revision)
  79. 2C-D‏‎ (1 revision)
  80. 60S ribosomal protein L7a‏‎ (1 revision)
  81. 40S ribosomal protein S13‏‎ (1 revision)
  82. 60S ribosomal protein L26‏‎ (1 revision)
  83. 4-HO-DET‏‎ (1 revision)
  84. 3C-P‏‎ (1 revision)
  85. 5150 (Involuntary psychiatric hold)‏‎ (1 revision)
  86. 22q11.2 deletion syndrome echocardiography or ultrasound‏‎ (1 revision)
  87. 3-Aminoisobutyric acid‏‎ (1 revision)
  88. 4-HO-pyr-T‏‎ (1 revision)
  89. 5-hydroxytryptophan‏‎ (1 revision)
  90. 5-Lipoxygenase activating protein‏‎ (1 revision)
  91. 60S ribosomal protein L30‏‎ (1 revision)
  92. 3-Aminopyridine‏‎ (1 revision)
  93. 4-HO-MPT‏‎ (1 revision)
  94. 22q11.2 deletion syndrome case study one‏‎ (1 revision)
  95. ABCC4‏‎ (1 revision)
  96. 5-MeS-DMT‏‎ (1 revision)
  97. 23andMe‏‎ (1 revision)
  98. 3-hydroxyacyl-coenzyme A dehydrogenase deficiency‏‎ (1 revision)
  99. 5-alpha-reductase deficiency secondary prevention‏‎ (1 revision)
  100. 310 helix‏‎ (1 revision)

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