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Page 1
Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height.
Oncotarget. 2011 Dec;2(12):1127-33. doi: 10.18632/oncotarget.385.
Oncotarget. 2011.
PMID: 22190405
Free PMC article.
Two pregnancies in a woman with Williams syndrome.
Mulik VV, Temple KI, Howe DT.
Mulik VV, et al. Among authors: temple ki.
BJOG. 2004 May;111(5):511-2. doi: 10.1111/j.1471-0528.2004.00109.x.
BJOG. 2004.
PMID: 15104621
No abstract available.
Item in Clipboard
Supramolecular organometallic polymer chemistry: multiple morphologies and superstructures from the solution self-assembly of polyferrocene-block-polysiloxane-block-polyferrocene triblock copolymers.
Resendes R, Massey JA, Temple K, Cao L, Power-Billard KN, Winnik MA, Manners I.
Resendes R, et al.
Chemistry. 2001 Jun 1;7(11):2414-24. doi: 10.1002/1521-3765(20010601)7:11<2414::aid-chem24140>3.0.co;2-1.
Chemistry. 2001.
PMID: 11446644
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Skin spots and heart tumors.
Reddy TD, Eccles DM, Theaker J, Keeton BR, Temple K.
Reddy TD, et al.
J Pediatr. 2001 Dec;139(6):901-2. doi: 10.1067/mpd.2001.119595.
J Pediatr. 2001.
PMID: 11743523
No abstract available.
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Transition metal-catalyzed formation of boron-nitrogen bonds: catalytic dehydrocoupling of amine-borane adducts to form aminoboranes and borazines.
Jaska CA, Temple K, Lough AJ, Manners I.
Jaska CA, et al.
J Am Chem Soc. 2003 Aug 6;125(31):9424-34. doi: 10.1021/ja030160l.
J Am Chem Soc. 2003.
PMID: 12889973
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Neonatal diabetes in Ukraine: incidence, genetics, clinical phenotype and treatment.
Globa E, Zelinska N, Mackay DJ, Temple KI, Houghton JA, Hattersley AT, Flanagan SE, Ellard S.
Globa E, et al. Among authors: temple ki.
J Pediatr Endocrinol Metab. 2015 Nov 1;28(11-12):1279-86. doi: 10.1515/jpem-2015-0170.
J Pediatr Endocrinol Metab. 2015.
PMID: 26208381
Free PMC article.
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Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients.
Hoornaert KP, Vereecke I, Dewinter C, Rosenberg T, Beemer FA, Leroy JG, Bendix L, Björck E, Bonduelle M, Boute O, Cormier-Daire V, De Die-Smulders C, Dieux-Coeslier A, Dollfus H, Elting M, Green A, Guerci VI, Hennekam RC, Hilhorts-Hofstee Y, Holder M, Hoyng C, Jones KJ, Josifova D, Kaitila I, Kjaergaard S, Kroes YH, Lagerstedt K, Lees M, Lemerrer M, Magnani C, Marcelis C, Martorell L, Mathieu M, McEntagart M, Mendicino A, Morton J, Orazio G, Paquis V, Reish O, Simola KO, Smithson SF, Temple KI, Van Aken E, Van Bever Y, van den Ende J, Van Hagen JM, Zelante L, Zordania R, De Paepe A, Leroy BP, De Buyzere M, Coucke PJ, Mortier GR.
Hoornaert KP, et al. Among authors: temple ki.
Eur J Hum Genet. 2010 Aug;18(8):872-80. doi: 10.1038/ejhg.2010.23. Epub 2010 Feb 24.
Eur J Hum Genet. 2010.
PMID: 20179744
Free PMC article.
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Beta-cell dysfunction in classic transient neonatal diabetes is characterized by impaired insulin response to glucose but normal response to glucagon.
Valerio G, Franzese A, Salerno M, Muzzi G, Cecere G, Temple KI, Shield JP.
Valerio G, et al. Among authors: temple ki.
Diabetes Care. 2004 Oct;27(10):2405-8. doi: 10.2337/diacare.27.10.2405.
Diabetes Care. 2004.
PMID: 15451908
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