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
  • [21] 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, 90 : 2384 - 2389
  • [22] A sequence variant on 17q21 is associated with age at onset and severity of asthma
    Halapi, Eva
    Gudbjartsson, Daniel F.
    Jonsdottir, Gudrun M.
    Bjornsdottir, Unnur S.
    Thorleifsson, Gudmar
    Helgadottir, Hafdis
    Williams, Carolyn
    Koppelman, Gerard H.
    Heinzmann, Andrea
    Boezen, H. Marike
    Jonasdottir, Aslaug
    Blondal, Thorarinn
    Gudjonsson, Sigurjon A.
    Jonasdottir, Adalbjorg
    Thorlacius, Theodora
    Henry, Amanda P.
    Altmueller, Janine
    Krueger, Marcus
    Shin, Hyoung Doo
    Uh, Soo-Taek
    Cheong, Hyun Sub
    Jonsdottir, Brynja
    Ludviksson, Bjorn R.
    Ludviksdottir, Dora
    Gislason, David
    Park, Choon-Sik
    Deichmann, Klaus
    Thompson, Philip J.
    Wjst, Matthias
    Hall, Ian P.
    Postma, Dirkje S.
    Gislason, Thorarinn
    Kong, Augustine
    Jonsdottir, Ingileif
    Thorsteinsdottir, Unnur
    Stefansson, Kari
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2010, 18 (08) : 902 - 908
  • [23] The Distribution and Most Recent Common Ancestor of the 17q21 Inversion in Humans
    Donnelly, Michael P.
    Paschou, Peristera
    Grigorenko, Elena
    Gurwitz, David
    Mehdi, Syed Qasim
    Kajuna, Sylvester L. B.
    Barta, Csaba
    Kungulilo, Selemani
    Karoma, N. J.
    Lu, Ru-Band
    Zhukova, Olga V.
    Kim, Jong-Jin
    Comas, David
    Siniscalco, Marcello
    New, Maria
    Li, Peining
    Li, Hui
    Manolopoulos, Vangelis G.
    Speed, William C.
    Rajeevan, Haseena
    Pakstis, Andrew J.
    Kidd, Judith R.
    Kidd, Kenneth K.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2010, 86 (02) : 161 - 171
  • [24] HUMAN ADHALIN IS ALTERNATIVELY SPLICED AND THE GENE IS LOCATED ON CHROMOSOME 17Q21
    MCNALLY, EM
    YOSHIDA, M
    MIZUNO, Y
    OZAWA, E
    KUNKEL, LM
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (21) : 9690 - 9694
  • [25] Loss of heterozygosity in the 17q21 region in breast cancer: clinical correlation
    GarciaPatino, E
    Gomendio, B
    Provencio, M
    Silva, JM
    Garcia, JM
    Lianes, P
    Palacios, J
    Espana, P
    Bonilla, F
    BREAST, 1997, 6 (05) : P903 - P903
  • [26] Replication of autism linkage:: Fine-mapping peak at 17q21
    Cantor, RM
    Kono, N
    Duvall, JA
    Alvarez-Retuerto, A
    Stone, JL
    Alarcón, M
    Nelson, SF
    Geschwind, DH
    AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (06) : 1050 - 1056
  • [27] Candidate target genes for loss of heterozygosity on human chromosome 17q21
    DeMarchis, L
    Cropp, C
    Sheng, ZM
    Bargo, S
    Callahan, R
    BRITISH JOURNAL OF CANCER, 2004, 90 (12) : 2384 - 2389
  • [28] Decreased sphingolipid synthesis in children with 17q21 asthma risk genotypes
    Ono, Jennie G.
    Kim, Benjamin, I
    Zhao, Yize
    Christos, Paul J.
    Tesfaigzi, Yohannes
    Worgall, Tilla S.
    Worgall, Stefan
    JOURNAL OF CLINICAL INVESTIGATION, 2020, 130 (02) : 921 - 926
  • [29] Common variants at 6q22 and 17q21 are associated with intracranial volume
    Nature Genetics, 2012, 44 : 539 - 544
  • [30] Genetic diversity of North African populations in the 17q21 genomic region
    Messaoudi, Mohsen
    Pakstis, Andrew J.
    Ezzaher, Takwa
    Boussetta, Sami
    Ben Ammar Elgaaied, Amel
    Kidd, Kenneth K.
    Cherni, Lotfi
    MAMMALIAN GENOME, 2024, 35 (03) : 445 - 460
12345