Pages with the fewest revisions

Showing below up to 50 results in range #371 to #420.

371. 2β-propanoyl-3β-(4-tolyl)-tropane (1 revision)
372. ADAMTS12 (1 revision)
373. ADAM8 (1 revision)
374. ADAMTS4 (1 revision)
375. ADAMTS17 (1 revision)
376. 3,4-Diaminopyridine (1 revision)
377. 3,4-Dimethylamphetamine (1 revision)
378. ADAMTSL1 (1 revision)
379. 68W (1 revision)
380. 3-Aminoisobutyric acid (1 revision)
381. 3-Aminopyridine (1 revision)
382. ADARB2 (1 revision)
383. 3-Hydroxyacyl ACP dehydrase (1 revision)
384. ADEPT (1 revision)
385. 8-Hyydroxyquinoline (1 revision)
386. 3-Methylcrotonyl-CoA carboxylase deficiency (1 revision)
387. ADK (gene) (1 revision)
388. AFF3 (1 revision)
389. 3-Methylglutaconyl CoA (1 revision)
390. ADP-specific glucokinase (1 revision)
391. 3-Quinuclidinyl benzilate (1 revision)
392. 3-Ureidopropionic acid (1 revision)
393. 3-dehydrosphinganine reductase (1 revision)
394. AEBP2 (1 revision)
395. 3-hydroxy-3-methylglutaryl-CoA lyase deficiency (1 revision)
396. AFM (gene) (1 revision)
397. 8-cell stage (1 revision)
398. 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (1 revision)
399. 3-hydroxyisobutyrate dehydrogenase (1 revision)
400. AKR1C4 (1 revision)
401. 3-methylglutaconic acid (1 revision)
402. 310 helix (1 revision)
403. AGBL4 (1 revision)
404. AGMAT (1 revision)
405. 3C-P (1 revision)
406. AGPAT5 (1 revision)
407. 3T3-L1 (1 revision)
408. 4-HO-MET (1 revision)
409. 3 beta-hydroxysteroid dehydrogenase deficiency historical perspective (1 revision)
410. 3 hydroxyisobutyric aciduria (1 revision)
411. 3 methylcrotonic aciduria (1 revision)
412. 3c syndrome (1 revision)
413. 3m syndrome (1 revision)
414. AIC (gene) (1 revision)
415. 3β-(4'-chlorophenyl)-2β-(3'-phenylisoxazol-5'-yl)tropane (1 revision)
416. AIDA interactive educational freeware diabetes simulator (1 revision)
417. 4,5-MDO-DMT (1 revision)
418. 4,5-MDO-DiPT (1 revision)
419. ADCK3 (1 revision)
420. 9q34 deletion syndrome (1 revision)