These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
118 related items for PubMed ID: 23450469
21. Genome-wide scan in 124 Indonesian sib-pair families with schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21. IrmansyahDepartment of Psychiatry, Faculty of Medicine, University of Indonesia, Jakarta, Indonesia., Schwab SG, Heriani, Handoko HY, Kusumawardhani A, Widyawati I, Amir N, Nasrun MW, Holmans P, Knapp M, Wildenauer DB. Am J Med Genet B Neuropsychiatr Genet; 2008 Oct 05; 147B(7):1245-52. PubMed ID: 18449910 [Abstract] [Full Text] [Related]
22. Follow-up analysis of 180 Chinese Han families: identification of a novel locus for psoriasis at 2p22.3-11.2. Sun LD, Yang S, Liu JJ, Ren YQ, Fan X, Xu SX, Zhou L, Yang CJ, Xiao FL, Gao M, Cui Y, Du WH, Huang W, Zhang XJ. Br J Dermatol; 2008 Mar 05; 158(3):512-7. PubMed ID: 18241272 [Abstract] [Full Text] [Related]
23. Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method. Camp NJ, Neuhausen SL, Tiobech J, Polloi A, Coon H, Myles-Worsley M. Am J Hum Genet; 2001 Dec 05; 69(6):1278-89. PubMed ID: 11668428 [Abstract] [Full Text] [Related]
24. A genome-wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba. Marcheco-Teruel B, Flint TJ, Wikman FP, Torralbas M, González L, Blanco L, Tan Q, Ewald H, Orntoft T, Kruse TA, Børglum AD, Mors O. Am J Med Genet B Neuropsychiatr Genet; 2006 Dec 05; 141B(8):833-43. PubMed ID: 16917938 [Abstract] [Full Text] [Related]
25. Genome scan for locus involved in mandibular prognathism in pedigrees from China. Li Q, Zhang F, Li X, Chen F. PLoS One; 2010 Sep 10; 5(9):. PubMed ID: 20844756 [Abstract] [Full Text] [Related]
27. [A genome-wide screening for pathological myopia suggests a novel locus on chromosome 15q12 - 13]. Yu ZQ, Li YB, Huang CX, Chu RY, Hu DN, Shen ZH, Huang W. Zhonghua Yan Ke Za Zhi; 2007 Mar 10; 43(3):233-8. PubMed ID: 17605906 [Abstract] [Full Text] [Related]
29. Genome-wide linkage scan of quantitative traits representing symptom dimensions in multiplex schizophrenia families. Ryu S, Won HH, Oh S, Kim JW, Park T, Cho EY, Cho Y, Park DY, Lee YS, Kwon JS, Hong KS. Psychiatry Res; 2013 Dec 30; 210(3):756-60. PubMed ID: 24035701 [Abstract] [Full Text] [Related]
30. Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4. Feng BJ, Huang W, Shugart YY, Lee MK, Zhang F, Xia JC, Wang HY, Huang TB, Jian SW, Huang P, Feng QS, Huang LX, Yu XJ, Li D, Chen LZ, Jia WH, Fang Y, Huang HM, Zhu JL, Liu XM, Zhao Y, Liu WQ, Deng MQ, Hu WH, Wu SX, Mo HY, Hong MF, King MC, Chen Z, Zeng YX. Nat Genet; 2002 Aug 30; 31(4):395-9. PubMed ID: 12118254 [Abstract] [Full Text] [Related]
32. Genome-wide linkage and regional association study of blood pressure response to the cold pressor test in Han Chinese: the genetic epidemiology network of salt sensitivity study. Yang X, Gu D, He J, Hixson JE, Rao DC, Lu F, Mu J, Jaquish CE, Chen J, Huang J, Shimmin LC, Rice TK, Chen J, Wu X, Liu D, Kelly TN. Circ Cardiovasc Genet; 2014 Aug 30; 7(4):521-8. PubMed ID: 25028485 [Abstract] [Full Text] [Related]
33. A genome-wide scan for the Sasang constitution in a Korean family suggests significant linkage at chromosomes 8q11.22-23 and 11q22.1-3. Won HH, Lee S, Jang E, Kim KK, Park YK, Kim YJ, Kim YS, Kim BY, Kim JY, Kim JW. J Altern Complement Med; 2009 Jul 30; 15(7):765-9. PubMed ID: 19552595 [Abstract] [Full Text] [Related]
36. [Linkage analysis of susceptibility loci in 2 target chromosomes in pedigrees with paranoid schizophrenia and undifferentiated schizophrenia]. Zeng LP, Hu ZM, Mu LL, Mei GS, Lu XL, Zheng YJ, Li PJ, Zhang YX, Pan Q, Long ZG, Dai HP, Zhang ZH, Xia JH, Zhao JP, Xia K. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun 30; 28(3):256-60. PubMed ID: 21644218 [Abstract] [Full Text] [Related]
37. Evidence for a novel autosomal dominant retinitis pigmentosa linked to chromosome 1p22.1-q12 in a Chinese family. Yuan Y, Zhou X, Wang F, Yan M, Ding F. Curr Eye Res; 2011 Feb 30; 36(2):154-67. PubMed ID: 21281067 [Abstract] [Full Text] [Related]
39. [Preliminary linkage analysis and mapping of keloid susceptibility locus in a Chinese pedigree]. Yan X, Gao JH, Chen Y, Song M, Liu XJ. Zhonghua Zheng Xing Wai Ke Za Zhi; 2007 Jan 30; 23(1):32-5. PubMed ID: 17393690 [Abstract] [Full Text] [Related]
40. Genome-wide scan identifies a susceptibility locus for familial primary cutaneous amyloidosis on chromosome 5p13.1-q11.2. Lee DD, Lin MW, Chen IC, Huang CY, Liu MT, Wang CR, Chang YT, Liu HN, Liu TT, Wong CK, Tsai SF. Br J Dermatol; 2006 Dec 30; 155(6):1201-8. PubMed ID: 17107390 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]