Mutation analysis of two candidate genes in the paroxysmal dystonic choreoathetosis locus on chromosome 2q.

被引：0
|
作者：
Tokarz, D [1 ]
Thomas, D [1 ]
Rainier, SR [1 ]
Fink, JK [1 ]
机构：
[1] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2001年 / 69卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2633
引用
收藏
页码：629 / 629
页数：1
相关论文
共 50 条
  • [21] Construction of a high-resolution physical map of the chromosome 10q22-q23 dilated cardiomyopathy locus and analysis of candidate genes
    Bowles, KR
    Abraham, SE
    Brugada, R
    Zintz, C
    Comeaux, J
    Sorajja, D
    Tsubata, S
    Li, H
    Brandon, L
    Gibbs, RA
    Scherer, SE
    Bowles, NE
    Towbin, JA
    GENOMICS, 2000, 67 (02) : 109 - 127
  • [22] Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes
    Annick Toutain
    Benoît Dessay
    Nathalie Ronce
    Maria-Immacolata Ferrante
    Julie Tranchemontagne
    Ruth Newbury-Ecob
    Carina Wallgren-Pettersson
    John Burn
    Josseline Kaplan
    Annick Rossi
    Silvia Russo
    Ian Walpole
    James K Hartsfield
    Nina Oyen
    Andrea Nemeth
    Pierre Bitoun
    Dorothy Trump
    Claude Moraine
    Brunella Franco
    European Journal of Human Genetics, 2002, 10 : 516 - 520
  • [23] Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes
    Toutain, A
    Dessay, B
    Ronce, N
    Ferrante, MI
    Tranchemontagne, J
    Newbury-Ecob, R
    Wallgren-Pettersson, C
    Burn, J
    Kaplan, J
    Rossi, A
    Russo, S
    Walpole, I
    Hartsfield, JK
    Oyen, N
    Nemeth, A
    Bitoun, P
    Trump, D
    Moraine, C
    Franco, B
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 (09) : 516 - 520
  • [24] Positional candidate genes for hypertension susceptibility in a region of linkage on chromosome 2q in two ethnic groups
    Klos, Kathy L.
    Barkley, Ruth Ann
    Mosley, Thomas H.
    Hanis, Craig L.
    Boerwinkle, Eric
    CIRCULATION, 2007, 116 (16) : 807 - 807
  • [25] Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes
    Andrew B West
    Alexander Zimprich
    Paul J Lockhart
    Matthew Farrer
    Andrew Singleton
    Benjamin Holtom
    Sarah Lincoln
    Anne Hofer
    Lori Hill
    Bertram Müller-Myhsok
    Zbigniew K Wszolek
    John Hardy
    Thomas Gasser
    European Journal of Human Genetics, 2001, 9 : 659 - 666
  • [26] Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes
    West, AB
    Zimprich, A
    Lockhart, PJ
    Farrer, M
    Singleton, A
    Holtom, B
    Lincoln, S
    Hofer, A
    Hill, L
    Müller-Myhsok, B
    Wszolek, ZK
    Hardy, J
    Gasser, T
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (09) : 659 - 666
  • [27] Mutation analyses of candidate genes detected by CGH on chromosome 16q in invasive breast carcinoma
    Schmidt, H.
    Hungermann, D.
    Agelopoulos, K.
    Korsching, E.
    Brandt, B.
    Boecker, W.
    Buerger, H.
    PATHOLOGY RESEARCH AND PRACTICE, 2007, 203 (05) : 262 - 262
  • [28] Mutation screening of candidate genes in the critical region of FDCM mapped to chromosome 1q32.
    Li, D
    Karibe, A
    Czemuszewicz, G
    Gonzalez, O
    Bachinski, L
    Roberts, R
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 304 - 304
  • [29] Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genes
    Michielse, Caroline B.
    Bhat, Meena
    Brady, Angela
    Jafrid, Hussain
    van den Hurk, Jose A. J. M.
    Raashid, Yasmin
    Brunner, Han G.
    van Bokhoven, Hans
    Padberg, George W.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2006, 14 (12) : 1306 - 1312
  • [30] Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genes
    Caroline B Michielse
    Meena Bhat
    Angela Brady
    Hussain Jafrid
    José A J M van den Hurk
    Yasmin Raashid
    Han G Brunner
    Hans van Bokhoven
    George W Padberg
    European Journal of Human Genetics, 2006, 14 : 1306 - 1312
12345