Linkage mapping of a gene for familial partial lipodystrophy to chromosome 1p11-q24.

被引:0
|
作者
Peters, JM [1 ]
Barnes, B [1 ]
Gitomer, W [1 ]
Bennett, L [1 ]
Garg, A [1 ]
Bowcock, AM [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dallas, TX USA
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
1696
引用
收藏
页码:A291 / A291
页数:1
相关论文
共 50 条
  • [41] FAMILIAL PARTIAL TRISOMY OF LONG ARM OF CHROMOSOME-10 (Q24-26)
    MORENOFUENMAYOR, H
    ZACKAI, EH
    MELLMAN, WJ
    ARONSON, M
    PEDIATRICS, 1975, 56 (05) : 756 - 761
  • [42] Linkage and radiation hybrid mapping of the porcine calsequestrin 1 (CASQ1) gene to chromosome 4q
    Knoll, A
    Stratil, A
    Reiner, G
    Peelman, LJ
    Van Poucke, M
    Geldermann, H
    ANIMAL GENETICS, 2002, 33 (05) : 390 - 392
  • [43] Familial partial epilepsy with variable foci in a Spanish family with linkage to chromosome 22q12
    Morales-Corraliza, J
    Gomez-Garre, P
    Gutierrez-Delicado, E
    Diaz-Otero, F
    Serratosa, JM
    EPILEPSIA, 2003, 44 : 166 - 167
  • [44] Familial partial epilepsy with variable foci:: Clinical features and linkage to chromosome 22q12
    Berkovic, SF
    Serratosa, JM
    Phillips, HA
    Xiong, L
    Andermann, E
    Díaz-Otero, F
    Gómez-Garre, P
    Martín, M
    Fernández-Bullido, Y
    Andermann, F
    Lopes-Cendes, I
    Dubeau, F
    Desbiens, R
    Scheffer, IE
    Wallace, RH
    Mulley, JC
    Pandolfo, J
    EPILEPSIA, 2004, 45 (09) : 1054 - 1060
  • [45] Human rod monochromacy:: Linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11
    Wissinger, B
    Jägle, H
    Kohl, S
    Broghammer, M
    Baumann, B
    Hanna, DB
    Hedels, C
    Apfelstedt-Sylla, E
    Randazzo, G
    Jacobson, SG
    Zrenner, E
    Sharpe, LT
    GENOMICS, 1998, 51 (03) : 325 - 331
  • [46] Linkage and radiation hybrid mapping of the porcine MPZ gene to chromosome 4q
    Wagenknecht, D
    Bartenschlager, H
    Van Poucke, M
    Geldermann, H
    Peelman, LJ
    Majzlík, I
    Stratil, A
    ANIMAL GENETICS, 2005, 36 (02) : 181 - 182
  • [47] Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13
    Magré, J
    Delépine, M
    Khallouf, E
    Gedde-Dahl, T
    Van Maldergem, L
    Sobel, E
    Papp, J
    Meier, M
    Mégarbané, A
    Lathrop, M
    Capeau, J
    NATURE GENETICS, 2001, 28 (04) : 365 - 370
  • [48] MAPPING OF A GENE DETERMINING TUBEROUS SCLEROSIS TO HUMAN CHROMOSOME-11Q14-11Q23
    SMITH, M
    SMALLEY, S
    CANTOR, R
    PANDOLFO, M
    GOMEZ, MI
    BAUMANN, R
    FLODMAN, P
    YOSHIYAMA, K
    NAKAMURA, Y
    JULIER, C
    DUMARS, K
    HAINES, J
    TROFATTER, J
    SPENCE, MA
    WEEKS, D
    CONNEALLY, M
    GENOMICS, 1990, 6 (01) : 105 - 114
  • [49] Linkage and association mapping of a chromosome 1q21-q24 type 2 diabetes susceptibility locus in Northern European Caucasians
    Das, SK
    Hasstedt, SJ
    Zhang, ZX
    Elbein, SC
    DIABETES, 2004, 53 (02) : 492 - 499
  • [50] Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes
    Rebecca C. J. Twells
    Charles A. Mein
    Felicity Payne
    Riitta Veijola
    Matthew Gilbey
    Matthew Bright
    Andrew Timms
    Yusuke Nakagawa
    Hywel Snook
    Sarah Nutland
    Helen E. Rance
    Philippa Carr
    Frank Dudbridge
    Heather J. Cordell
    Jason Cooper
    Eva Tuomilehto-Wolf
    Jaakko Tuomilehto
    Michael Phillips
    Michael Metzker
    J. Fred Hess
    John A. Todd
    Human Genetics, 2003, 113 : 99 - 105