CARRIER DETECTION AND CHARACTERIZATION OF GENE DELETIONS IN DUCHENNE AND BECKER MUSCULAR-DYSTROPHY UTILIZING DYSTROPHIN CDNA PROBES

被引：0
|
作者：
PRIOR, TW
FRIEDMAN, KJ
SILVERMAN, LM
机构：
[1] UNIV N CAROLINA,DEPT PATHOL,CHAPEL HILL,NC 27599
[2] UNIV N CAROLINA,HOSP LABS,CHAPEL HILL,NC 27599
[3] N CAROLINA MEM HOSP,DEPT PATHOL,CHAPEL HILL,NC 27599
[4] N CAROLINA MEM HOSP,HOSP LABS,CHAPEL HILL,NC 27599
来源：
CLINICAL CHEMISTRY | 1989年 / 35卷 / 06期
关键词：
D O I：
暂无
中图分类号：
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号：
1001 ;
摘要：
引用
收藏
页码：1075 / 1075
页数：1
相关论文
共 50 条
  • [21] Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy
    Florencia, G
    Verónica, F
    Viviana, D
    Irene, S
    NEUROLOGICAL RESEARCH, 2004, 26 (01) : 83 - 87
  • [22] DETECTION OF GENE DELETIONS AND DIAGNOSIS OF DUCHENNE MUSCULAR-DYSTROPHY
    GRANINGER, W
    WINTERSBERGER, W
    MERON, G
    SMOLEN, J
    TOIFL, K
    VORMITTAG, W
    WIENER KLINISCHE WOCHENSCHRIFT, 1991, 103 (07) : 207 - 209
  • [23] APPLICATION OF DNA PROBES TO CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF DUCHENNE (AND BECKER) MUSCULAR-DYSTROPHY
    MULLEY, JC
    GEDEON, AK
    HAAN, EA
    SHEFFIELD, LJ
    WHITE, SJ
    BATES, LJ
    ROBERTSON, EF
    SUTHERLAND, GR
    AUSTRALIAN PAEDIATRIC JOURNAL, 1988, 24 : 92 - 97
  • [24] INTRAGENIC DELETIONS IN 164 BOYS WITH DUCHENNE MUSCULAR-DYSTROPHY (DMD) STUDIED WITH DYSTROPHIN CDNA
    UPADHYAYA, M
    SMITH, RA
    THOMAS, NST
    NORMAN, AM
    HARPER, PS
    CLINICAL GENETICS, 1990, 37 (06) : 456 - 462
  • [25] SOMATIC MOSAICISM FOR A DELETION OF THE DYSTROPHIN GENE IN A CARRIER OF BECKER MUSCULAR-DYSTROPHY
    VOIT, T
    NEUENJACOB, E
    MAHLER, V
    JAUCH, A
    CREMER, M
    EUROPEAN JOURNAL OF PEDIATRICS, 1992, 151 (02) : 112 - 116
  • [26] DYSTROPHIN IMMUNOHISTOCHEMISTRY IN A SYMPTOMATIC CARRIER OF BECKER MUSCULAR-DYSTROPHY
    HAGINOYA, K
    YAMAMOTO, K
    IINUMA, K
    YANAGISAWA, T
    ICHINOHASAMA, Y
    SHIMMOTO, M
    SUZUKI, Y
    TADA, K
    JOURNAL OF NEUROLOGY, 1991, 238 (07) : 375 - 378
  • [27] Detection of deletions in the dystrophin gene in Duchenne-Becker muscular dystrophy by the multiple polymerase chain reaction
    Horvathova, L
    Hubertova, K
    Kadasi, L
    Simko, J
    CESKA A SLOVENSKA NEUROLOGIE A NEUROCHIRURGIE, 1996, 59 (04) : 201 - 205
  • [28] HETEROGENEITY OF DYSTROPHIN EXPRESSION IN PATIENTS WITH DUCHENNE AND BECKER MUSCULAR-DYSTROPHY
    NICHOLSON, LVB
    JOHNSON, MA
    GARDNERMEDWIN, D
    BHATTACHARYA, S
    HARRIS, JB
    ACTA NEUROPATHOLOGICA, 1990, 80 (03) : 239 - 250
  • [29] DYSTROPHIN IMMUNOCYTOCHEMISTRY IN MUSCLE CULTURE - DETECTION OF A CARRIER OF DUCHENNE MUSCULAR-DYSTROPHY
    MIRANDA, AF
    FRANCKE, U
    BONILLA, E
    MARTUCCI, G
    SCHMIDT, B
    SALVIATI, G
    RUBIN, M
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 32 (02): : 268 - 273
  • [30] POSSIBILITIES AND LIMITATION OF PRENATAL-DIAGNOSIS AND CARRIER DETERMINATION FOR DUCHENNE AND BECKER MUSCULAR-DYSTROPHY USING CDNA PROBES
    SPEER, A
    SPIEGLER, AWJ
    HANKE, R
    GRADE, K
    GIERTLER, U
    SCHIECK, J
    FORREST, S
    DAVIES, KE
    NEUMANN, R
    BOLLMANN, R
    BOMMER, C
    SOMMER, D
    COUTELLE, C
    JOURNAL OF MEDICAL GENETICS, 1989, 26 (01) : 1 - 5
12345