Human HRK gene maps to position 12q13.1

被引:0
|
作者
O. V. Muravenko
V. I. Kashuba
A. S. Kutsenko
R. Z. Gizatullin
A. I. Protopopov
S. M. Kvasha
A. N. Al-Amin
A. V. Zelenin
E. R. Zabarovsky
机构
[1] Engelhardt Institute of Molecular Biology,Center for Genomics Research and Microbiology and Tumor Biology Center
[2] Karolinska Institute,undefined
来源
Chromosome Research | 2000年 / 8卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:656 / 656
相关论文
共 50 条
  • [41] EVIDENCE FOR LINKAGE OF THE CENTRAL CORE DISEASE LOCUS TO HUMAN CHROMOSOME-19Q12-13.1
    KAUSCH, K
    LEHMANNHORN, F
    GRIMM, T
    JANKA, M
    WIERINGA, B
    MUELLER, CR
    CYTOGENETICS AND CELL GENETICS, 1991, 58 (3-4): : 2020 - 2020
  • [42] THE HUMAN CORTICOTROPIN-RELEASING FACTOR-RECEPTOR (CRHR) GENE MAPS TO CHROMOSOME 17Q12-Q22
    POLYMEROPOULOS, MH
    TORRES, R
    YANOVSKI, JA
    CHANDRASEKHARAPPA, SC
    LEDBETTER, DH
    GENOMICS, 1995, 28 (01) : 123 - 124
  • [43] THE HUMAN TISSUE TRANSGLUTAMINASE GENE MAPS ON CHROMOSOME-20Q12 BY IN-SITU FLUORESCENCE HYBRIDIZATION
    GENTILE, V
    DAVIES, PJA
    BALDINI, A
    GENOMICS, 1994, 20 (02) : 295 - 297
  • [44] Association of syndromic mental retardation with an Xq12q13.1 duplication encompassing the oligophrenin 1 gene
    Bedeschi, Maria Francesca
    Novelli, Antonio
    Bernardini, Laura
    Parazzini, Cecilia
    Bianchi, Vera
    Torres, Barbara
    Natacci, Federica
    Giuffrida, Maria Grazia
    Ficarazzi, Paola
    Dallapiccola, Bruno
    Lalatta, Faustina
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (13) : 1718 - 1724
  • [45] A gene for ataxic cerebral palsy maps to chromosome 9p12-q12
    McHale, DP
    Jackson, AP
    Campbell, DA
    Levene, MI
    Corry, P
    Woods, CG
    Lench, NJ
    Mueller, RF
    Markham, AF
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2000, 8 (04) : 267 - 272
  • [46] Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1
    Bento, J. L.
    Palmer, N. D.
    Zhong, M.
    Roh, B.
    Lewis, J. P.
    Wing, M. R.
    Pandya, H.
    Freedman, B. I.
    Langefeld, C. D.
    Rich, S. S.
    Bowden, D. W.
    Mychaleckyj, J. C.
    GENOMICS, 2008, 92 (04) : 226 - 234
  • [47] A gene for FG syndrome maps in the Xq12-q21.31 region
    Briault, S
    Hill, R
    Shrimpton, A
    Zhu, DP
    Till, M
    Ronce, N
    MargaritteJeannin, P
    Baraitser, M
    MiddletonPrice, H
    Malcolm, S
    Thompson, E
    Hoo, J
    Wilson, G
    Romano, C
    Guichet, A
    Pembrey, M
    Fontes, M
    Poustka, A
    Moraine, C
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 73 (01): : 87 - 90
  • [48] A gene for pili annulati maps to the telomeric region of chromosome 12q
    Green, J
    Fitzpatrick, E
    de Berker, C
    Forrest, SM
    Sinclair, RD
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2004, 123 (06) : 1070 - 1072
  • [49] ASSIGNMENT OF THE HUMAN HIPPOCAMPAL INWARD RECTIFIER POTASSIUM CHANNEL (HIR) GENE TO 22Q13.1
    BUDARF, ML
    PERIER, F
    BARNOSKI, BL
    BELL, CJ
    VANDENBERG, CA
    GENOMICS, 1995, 26 (03) : 625 - 629
  • [50] Characterization of the human and rat phospholemman (PLM) cDNAs and localization of the human PLM gene to chromosome 19q13.1
    Chen, LSK
    Lo, CF
    Numann, R
    Cuddy, M
    GENOMICS, 1997, 41 (03) : 435 - 443