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Results 1 - 10 of 103 for Tm
  1. ... NG, Forsen T, Fox C, Fraser RM, Frayling TM, Froguel P, Frossard P, Gao Y, Gertow K, ... AC, Takayanagi R, Takeuchi F, Tay WT, Teslovich TM, Thorand B, Thorleifsson G, Thorsteinsdottir U, Tikkanen E, ...
  2. ... Citation on PubMed Rose CD, Arostegui JI, Martin TM, Espada G, Scalzi L, Yague J, Rosenbaum JT, ... Free article on PubMed Central Rose CD, Doyle TM, McIlvain-Simpson G, Coffman JE, Rosenbaum JT, Davey ...
  3. ... Dhalaan H, al Zayed Z, Hellani A, Bosley TM. Five new consanguineous families with horizontal gaze palsy ... Epub 2008 Oct 1. Citation on PubMed Bosley TM, Salih MA, Jen JC, Lin DD, Oystreck D, ...
  4. ... N, Bangs R, Boorjian SA, Buyyounouski MK, Downs TM, Efstathiou JA, Friedlander T, Greenberg RE, Guru KA, ... C, Ojesina AI, Bullman S, Leraas KM, Lichtenberg TM, Wu CJ, Schultz N, Getz G, Meyerson M, ...
  5. ... KT, Hall IP, Sayers I, Tobin MD, Maher TM, Cho MH, Hunninghake GM, Schwartz DA, Yaspan BL, ... HL, Hart SP, Hill MR, Hirani N, Maher TM, McAnulty RJ, Millar AB, Molyneaux PL, Parfrey H, ...
  6. ... Free article on PubMed Central Schneider A, Bardakjian TM, Zhou J, Hughes N, Keep R, Dorsainville D, ... 12):2030. Citation on PubMed Williamson KA, Yates TM, FitzPatrick DR. SOX2 Disorder. 2006 Feb 23 [updated ...
  7. ... MUSCLES, CONGENITAL, 2; CFEOM2 TUKEL SYNDROME PubMed Bosley TM, Oystreck DT, Robertson RL, al Awad A, Abu- ... CJ, Awad AH, Zwaan J, Mullaney PB, Bosley TM, Engle EC. Homozygous mutations in ARIX(PHOX2A) result ...
  8. ... 1136/bcr-2014-204430. Citation on PubMed Miller TM, Dias da Silva MR, Miller HA, Kwiecinski H, ... wnl.0000143383.91137.00. Citation on PubMed Miller TM. Differential diagnosis of myotonic disorders. Muscle Nerve. 2008 ...
  9. ... Citation on PubMed Smith AC, Spuhler K, Williams TM, McConnell T, Sujansky E, Robinson A. Genetic risk ... 10.1002/ajmg.1320470415. Citation on PubMed Williams TM, McConnell TS, Martinez F Jr, Smith AC, Sujansky ...
  10. ... X, Warth R, Vilsen B, Zennaro MC, Strom TM, Reincke M. Somatic mutations in ATP1A1 and ATP2B3 ... A, Steichen O, Beuschlein F, Boulkroun S, Strom TM, Monticone S, Amar L, Meatchi T, Mantero F, ...
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