A GENE FOR FAMILIAL JUVENILE NEPHRONOPHTHISIS (NPH) MAPS TO CHROMOSOME 2Q11.1-Q21.1

被引:0
|
作者
HILDEBRANDT, F [1 ]
SINGHSAWHNEY, I [1 ]
SCHNIEDERS, B [1 ]
CENTOFANTE, L [1 ]
WEBER, JL [1 ]
BRANDIS, M [1 ]
机构
[1] MARSHFIELD MED FDN,MARSHFIELD,WI
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
引用
收藏
页码:242 / 242
页数:1
相关论文
共 50 条
  • [31] A familial chordoma locus maps to chromosome 7q33.
    Yang, X
    Kelley, MJ
    Korczak, JF
    Sheridan, E
    Goldstein, AM
    Parry, DM
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 512 - 512
  • [32] Evidence that a locus for familial psoriasis maps to chromosome 4q
    Matthews, D
    Fry, L
    Powles, A
    Weber, J
    McCarthy, M
    Fisher, E
    Davies, K
    Williamson, R
    NATURE GENETICS, 1996, 14 (02) : 231 - 233
  • [33] A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3
    Pedro Fernandez
    Johanna Moolman-Smook
    Paul Brink
    Valerie Corfield
    Human Genetics, 2005, 118 : 133 - 137
  • [34] A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3
    Fernandez, P
    Moolman-Smook, J
    Brink, P
    Corfield, V
    HUMAN GENETICS, 2005, 118 (01) : 133 - 137
  • [35] A gene for familiar eosinophilia maps to chromosome 5q31-q33.
    Lin, AY
    Rioux, JD
    Nutman, T
    Daly, M
    Stone, V
    Nguyen, H
    Green, T
    Hudson, T
    Zimmerman, PA
    Fontaine, L
    Tucker, MA
    Lander, E
    Goldstein, AM
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A283 - A283
  • [36] Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3
    Hedera, P.
    Blair, M. A.
    Andermann, E.
    Andermann, F.
    D'Agostino, D.
    Taylor, K. A.
    Chahine, L.
    Pandolfo, M.
    Bradford, Y.
    Haines, J. L.
    Abou-Khalil, B.
    NEUROLOGY, 2007, 68 (24) : 2107 - 2112
  • [37] REFINED GENETIC-MAPPING OF A GENE FOR FAMILIAL JUVENILE NEPHRONOPHTHISIS (NPH1) AND PHYSICAL MAPPING OF LINKED MARKERS
    HILDEBRANDT, F
    SINGHSAWHNEY, I
    SCHNIEDERS, B
    PAPENFUSS, T
    BRANDIS, M
    GENOMICS, 1995, 25 (02) : 360 - 364
  • [38] A rare cause of hypopituitarism arising from a chromosome 2 deletion (2q14.1-2q21.1)
    Hamill, C. F.
    Lindsay, J. R.
    IRISH JOURNAL OF MEDICAL SCIENCE, 2017, 186 : S368 - S368
  • [39] THE GENE RESPONSIBLE FOR FAMILIAL HYPOCALCIURIC HYPERCALCEMIA MAPS TO CHROMOSOME-3Q IN 4 UNRELATED FAMILIES
    CHOU, YHW
    BROWN, EM
    LEVI, T
    CROWE, G
    ATKINSON, AB
    ARNQVIST, HJ
    TOSS, G
    EL-HAJJ FULEIHAN, G
    SEIDMAN, JG
    SEIDMAN, CE
    NATURE GENETICS, 1992, 1 (04) : 295 - 300
  • [40] Assignment of the human dUTPase gene (DUT) to chromosome 15q15-q21.1 by fluorescence in situ hybridization
    Cohen, D
    Heng, HHQ
    Shi, XM
    McIntosh, EM
    Tsui, LC
    Pearlman, RE
    GENOMICS, 1997, 40 (01) : 213 - 215