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PubMed (cited) for id: 300470
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Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations.
N Engl J Med. 2016 May 12;374(19):1853-63. doi: 10.1056/NEJMoa1507629. Epub 2016 Apr 27.
N Engl J Med. 2016.
PMID: 27120771
Free article.
The DNA sequence of the human X chromosome.
Ross MT, Grafham DV, Coffey AJ, Scherer S, McLay K, Muzny D, Platzer M, Howell GR, Burrows C, Bird CP, Frankish A, Lovell FL, Howe KL, Ashurst JL, Fulton RS, Sudbrak R, Wen G, Jones MC, Hurles ME, Andrews TD, Scott CE, Searle S, Ramser J, Whittaker A, Deadman R, Carter NP, Hunt SE, Chen R, Cree A, Gunaratne P, Havlak P, Hodgson A, Metzker ML, Richards S, Scott G, Steffen D, Sodergren E, Wheeler DA, Worley KC, Ainscough R, Ambrose KD, Ansari-Lari MA, Aradhya S, Ashwell RI, Babbage AK, Bagguley CL, Ballabio A, Banerjee R, Barker GE, Barlow KF, Barrett IP, Bates KN, Beare DM, Beasley H, Beasley O, Beck A, Bethel G, Blechschmidt K, Brady N, Bray-Allen S, Bridgeman AM, Brown AJ, Brown MJ, Bonnin D, Bruford EA, Buhay C, Burch P, Burford D, Burgess J, Burrill W, Burton J, Bye JM, Carder C, Carrel L, Chako J, Chapman JC, Chavez D, Chen E, Chen G, Chen Y, Chen Z, Chinault C, Ciccodicola A, Clark SY, Clarke G, Clee CM, Clegg S, Clerc-Blankenburg K, Clifford K, Cobley V, Cole CG, Conquer JS, Corby N, Connor RE, David R, Davies J, Davis C, Davis J, Delgado O, Deshazo D, Dhami P, Ding Y, Dinh H, Dodsworth S, Draper H, Dugan-Rocha S, Dunham A, Dunn M, Durbin KJ, Dutta I, Eades T, Ellwood M, Eme…
See abstract for full author list ➔
Ross MT, et al.
Nature. 2005 Mar 17;434(7031):325-37. doi: 10.1038/nature03440.
Nature. 2005.
PMID: 15772651
Free PMC article.
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Expression pattern and further characterization of human MAGED2 and identification of rodent orthologues.
Langnaese K, Kloos DU, Wehnert M, Seidel B, Wieacker P.
Langnaese K, et al.
Cytogenet Cell Genet. 2001;94(3-4):233-40. doi: 10.1159/000048822.
Cytogenet Cell Genet. 2001.
PMID: 11856887
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A new MAGE gene with ubiquitous expression does not code for known MAGE antigens recognized by T cells.
Lucas S, Brasseur F, Boon T.
Lucas S, et al.
Cancer Res. 1999 Aug 15;59(16):4100-3.
Cancer Res. 1999.
PMID: 10463614
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Neonatal Bartter syndrome: spontaneous resolution of all signs and symptoms.
Reinalter S, Devlieger H, Proesmans W.
Reinalter S, et al.
Pediatr Nephrol. 1998 Apr;12(3):186-8. doi: 10.1007/s004670050433.
Pediatr Nephrol. 1998.
PMID: 9630034
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