TRISOMY-5P CAUSED BY FAMILIAL TRANSLOCATION

被引:0
|
作者
PALMA, V
GARCIA, B
CALVA, P
GUIZAR, J
SALAMANCA, F
机构
来源
ARCHIVOS DE INVESTIGACION MEDICA | 1985年 / 16卷 / 02期
关键词
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
引用
收藏
页码:29 / 29
页数:1
相关论文
共 50 条
  • [1] TRISOMY-5P SYNDROME
    RODEWALD, A
    JOURNAL OF MEDICAL GENETICS, 1979, 16 (05) : 406 - 406
  • [2] PARTIAL TRISOMY-5P
    YUNIS, E
    SILVA, R
    EGEL, H
    ZUNIGA, R
    DECABALLERO, OMT
    RAMIREZ, E
    DERUIZ, HP
    HUMAN GENETICS, 1978, 43 (02) : 231 - 237
  • [3] COMPLETE TRISOMY-5P - REPLY
    BRIMBLECOMBE, FSW
    VOWLES, M
    JOURNAL OF MEDICAL GENETICS, 1978, 15 (04) : 319 - 319
  • [4] 5 FAMILIAL CASES WITH A TRISOMY 16P-SYNDROME DUE TO TRANSLOCATION
    LESCHOT, NJ
    DENEF, JJ
    GERAEDTS, JPM
    BECKERBLOEMKOLK, MJ
    TALMA, A
    BIJLSMA, JB
    VERJAAL, M
    CLINICAL GENETICS, 1979, 16 (03) : 205 - 214
  • [5] Monosomy 5p and trisomy 12p in a boy with familial balanced translocation
    Vasudevan, Pradeep C.
    Parker, Michael J.
    CLINICAL DYSMORPHOLOGY, 2006, 15 (02) : 85 - 87
  • [6] FAMILIAL PARTIAL TRISOMY 5P RESULTING FROM SEGREGATION OF AN INSERTIONAL TRANSLOCATION
    GUSTAVSON, KH
    LUNDBERG, PO
    NICOL, P
    CLINICAL GENETICS, 1988, 33 (06) : 404 - 409
  • [7] FAMILIAL CHROMOSOMAL TRANSLOCATION LEADING TO A PARTIAL TRISOMY-1P
    SCHURMANN, M
    WETHLING, H
    NIEMEYER, ML
    SCHWINGER, E
    KLINISCHE PADIATRIE, 1987, 199 (01): : 27 - 31
  • [8] PHENOTYPE OF PATIENTS AT DIFFERENT AGES WITH PARTIAL TRISOMY 3P - A FAMILIAL TRANSLOCATION 3/5
    SCHWANITZ, G
    ZERRES, K
    ANNALES DE GENETIQUE, 1984, 27 (03): : 167 - 172
  • [9] Trisomy 12p syndrome secondary to a balanced familial translocation
    Gazzola Zen, Paulo Ricardo
    Machado Rosa, Rafael Fabiano
    Manique Rosa, Rosana Cardoso
    Graziadio, Carla
    Paskulin, Giorgio Adriano
    PEDIATRICS INTERNATIONAL, 2010, 52 (03) : e144 - e146
  • [10] COMPLETE TRISOMY-5P OWING TO DENOVO TRANSLOCATION T(5-22)(Q11-P11) WITH ISOCHROMOSOME-5P ASSOCIATED WITH A FAMILIAL PERICENTRIC-INVERSION OF CHROMOSOME-2, INV 2(P21Q11)
    ORYE, E
    BENOIT, Y
    VANMELE, B
    JOURNAL OF MEDICAL GENETICS, 1983, 20 (05) : 394 - 396