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au.\*:("KWON, Jennifer M")

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Prophylactic Phenobarbital Administration After Resolution of Neonatal Seizures : Survey of Current PracticeGUILLET, Ronnie; KWON, Jennifer M.Pediatrics (Evanston). 2008, Vol 122, Num 4, pp 731-735, issn 0031-4005, 5 p.Article

Brain-derived neurotrophic factor and autoantibodies to neural antigens in sera of children with autistic spectrum disorders, landau-kleffner syndrome, and epilepsyCONNOLLY, Anne M; CHEZ, Michael; STREIF, Elizabeth M et al.Biological psychiatry (1969). 2006, Vol 59, Num 4, pp 354-363, issn 0006-3223, 10 p.Article

Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's diseaseABRAHAM, Richard; MYERS, Amanda; KWON, Jennifer M et al.Human genetics. 2001, Vol 109, Num 6, pp 646-652, issn 0340-6717Article

Females experience a more severe disease course in batten diseaseCIALONE, Jennifer; ADAMS, Heather; RAMIREZ-MONTEALEGRE, Denia et al.Journal of inherited metabolic disease. 2012, Vol 35, Num 3, pp 549-555, issn 0141-8955, 7 p.Article

Evidence of common and specific genetic effects: association of the muscarinic acetylcholine receptor M2 (CHRM2) gene with alcohol dependence and major depressive syndromeWANG, Jen C; HINRICHS, Anthony L; JONES, Kevin et al.Human molecular genetics (Print). 2004, Vol 13, Num 17, pp 1903-1911, issn 0964-6906, 9 p.Article

Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathyVERHOEVEN, Kristien; DE JONGHE, Peter; VAN GERWEN, Veerle et al.American journal of human genetics. 2003, Vol 72, Num 3, pp 722-727, issn 0002-9297, 6 p.Article

Association studies using novel polymorphisms in BACEI and BACE2NOWOTNY, Petra; KWON, Jennifer M; CHAKRAVERTY, Sumi et al.Neuroreport (Oxford). 2001, Vol 12, Num 9, pp 1799-1802, issn 0959-4965Article

Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependenceHINRICHS, Anthony L; WANG, Jen C; FOROUD, Tatiana et al.American journal of human genetics. 2006, Vol 78, Num 1, pp 103-111, issn 0002-9297, 9 p.Article

Novel CLN3 mutation predicted to cause complete loss of protein function does not modify the classical JNCL phenotypeKWON, Jennifer M; ROFFIBERG, Paul G; LEMAN, Adam R et al.Neuroscience letters. 2005, Vol 387, Num 2, pp 111-114, issn 0304-3940, 4 p.Article

A genome screen of maximum number of drinks as an alcoholism phenotypeSACCONE, Nancy L; KWON, Jennifer M; RICE, John P et al.American journal of medical genetics. 2000, Vol 96, Num 5, pp 632-637, issn 0148-7299Article

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