A POSSIBLE NEW FRAGILE SITE AT 17Q21

被引:0
作者
ZHOU, XT
XU, BH
XIAO, GF
机构
来源
KEXUE TONGBAO | 1988年 / 33卷 / 02期
关键词
D O I
暂无
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
引用
收藏
页码:154 / 158
页数:5
相关论文
共 50 条
  • [41] Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume
    M Arfan Ikram
    Myriam Fornage
    Albert V Smith
    Sudha Seshadri
    Reinhold Schmidt
    Stéphanie Debette
    Henri A Vrooman
    Sigurdur Sigurdsson
    Stefan Ropele
    H Rob Taal
    Dennis O Mook-Kanamori
    Laura H Coker
    W T Longstreth
    Wiro J Niessen
    Anita L DeStefano
    Alexa Beiser
    Alex P Zijdenbos
    Maksim Struchalin
    Clifford R Jack
    Fernando Rivadeneira
    Andre G Uitterlinden
    David S Knopman
    Anna-Liisa Hartikainen
    Craig E Pennell
    Elisabeth Thiering
    Eric A P Steegers
    Hakon Hakonarson
    Joachim Heinrich
    Lyle J Palmer
    Marjo-Riitta Jarvelin
    Mark I McCarthy
    Struan F A Grant
    Beate St Pourcain
    Nicholas J Timpson
    George Davey Smith
    Ulla Sovio
    Mike A Nalls
    Rhoda Au
    Albert Hofman
    Haukur Gudnason
    Aad van der Lugt
    Tamara B Harris
    William M Meeks
    Meike W Vernooij
    Mark A van Buchem
    Diane Catellier
    Vincent W V Jaddoe
    Vilmundur Gudnason
    B Gwen Windham
    Philip A Wolf
    Nature Genetics, 2012, 44 : 732 - 732
  • [42] 17q21 variants modify the association between early respiratory infections and asthma
    Smit, L. A. M.
    Bouzigon, E.
    Pin, I.
    Siroux, V.
    Monier, F.
    Aschard, H.
    Bousquet, J.
    Gormand, F.
    Just, J.
    Le Moual, N.
    Nadif, R.
    Scheinmann, P.
    Vervloet, D.
    Lathrop, M.
    Demenais, F.
    Kauffmann, F.
    EUROPEAN RESPIRATORY JOURNAL, 2010, 36 (01) : 57 - 64
  • [43] Erratum: Candidate target genes for loss of heterozygosity on human chromosome 17q21
    L DeMarchis
    C Cropp
    Z M Sheng
    S Bargo
    R Callahan
    British Journal of Cancer, 2004, 91 : 1001 - 1001
  • [44] 17q21 variants are strongly associated with persistence of symptoms in young children with wheeze
    Granell, Raquel
    Sterne, Jonathan
    Henderson, John
    EUROPEAN RESPIRATORY JOURNAL, 2016, 48
  • [45] 17q21 locus and ORMDL3: an increased risk for childhood asthma
    Jennie G. Ono
    Tilla S. Worgall
    Stefan Worgall
    Pediatric Research, 2014, 75 : 165 - 170
  • [46] FREQUENCY AND CHARACTERIZATION OF TETRANUCLEOTIDE REPEAT POLYMORPHISMS ON CHROMOSOME-17 AND ISOLATION OF STRS FROM 17Q21
    BENNETTBAKER, PE
    KIOUSIS, S
    KUKOWSKALATALLO, JF
    DOJKA, MA
    CHAMBERLAIN, JS
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 976 - 976
  • [47] 17q21 locus and ORMDL3: an increased risk for childhood asthma
    Ono, Jennie G.
    Worgall, Tilla S.
    Worgall, Stefan
    PEDIATRIC RESEARCH, 2014, 75 (01) : 165 - 170
  • [48] Chromosome 17q21 markers are associated with quantitative asthma traits in Chinese children
    Leung, T.
    Sy, H.
    Chan, I
    Wong, G.
    Tang, N.
    Waye, M.
    Lam, C.
    ALLERGY, 2009, 64 : 103 - 104
  • [49] GENETIC-MAPPING OF THE BRCA1 REGION ON CHROMOSOME 17Q21
    ALBERTSEN, H
    PLAETKE, R
    BALLARD, L
    FUJIMOTO, E
    CONNOLLY, J
    LAWRENCE, E
    RODRIGUEZ, P
    ROBERTSON, M
    BRADLEY, P
    MILNER, B
    FUHRMAN, D
    MARKS, A
    SARGENT, R
    CARTWRIGHT, P
    MATSUNAMI, N
    WHITE, R
    AMERICAN JOURNAL OF HUMAN GENETICS, 1994, 54 (03) : 516 - 525
  • [50] Associations between the 17q21 region and allergic rhinitis in five birth cohorts
    Fuertes, Elaine
    Soderhall, Cilia
    Acevedo, Nathalie
    Becker, Allan
    Brauer, Michael
    Chan-Yeung, Moira
    Dijk, F. Nicole
    Heinrich, Joachim
    Koppelman, Gerard
    Postma, Dirkje
    Kere, Juha
    Kozyrskyj, Anita
    Pershagen, Goran
    Sandford, Andrew
    Standl, Marie
    Tiesler, Carla
    Waldenberger, Melanie
    Westman, Marit
    Carlsten, Christopher
    Melen, Erik
    EUROPEAN RESPIRATORY JOURNAL, 2014, 44