DNA STUDIES IN A FAMILY WITH DUCHENNE MUSCULAR-DYSTROPHY AND A DELETION AT XP21

被引:0
|
作者
GREENBERG, CR
HAMERTON, JL
NIGLI, M
WROGEMANN, K
机构
[1] UNIV MANITOBA,DEPT PEDIAT,WINNIPEG R3E 0W3,MANITOBA,CANADA
[2] UNIV MANITOBA,DEPT BIOCHEM,WINNIPEG R3E 0W3,MANITOBA,CANADA
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
引用
收藏
页码:128 / 137
页数:10
相关论文
共 50 条
  • [31] DUCHENNE MUSCULAR-DYSTROPHY - DATA FROM FAMILY STUDIES
    DANIELI, GA
    MOSTACCIUOLO, ML
    PILOTTO, G
    ANGELINI, C
    BONFANTE, A
    HUMAN GENETICS, 1980, 54 (01) : 63 - 68
  • [32] FURTHER EVIDENCE FOR XP21 LOCATION OF DUCHENNE MUSCULAR-DYSTROPHY (DMD) LOCUS - X-9 TRANSLOCATION IN A FEMALE WITH DMD
    EMANUEL, BS
    ZACKAI, EH
    TUCKER, SH
    JOURNAL OF MEDICAL GENETICS, 1983, 20 (06) : 461 - 463
  • [33] Pseudohypertrophy of the temporalis muscle in Xp21 muscular dystrophy
    Richards, P
    Saywell, WR
    Heywood, P
    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2000, 42 (11): : 786 - 787
  • [34] LOCALIZATION OF DNA-SEQUENCES IN REGION XP21 OF THE HUMAN X-CHROMOSOME - SEARCH FOR MOLECULAR MARKERS CLOSE TO THE DUCHENNE MUSCULAR-DYSTROPHY LOCUS
    DEMARTINVILLE, B
    KUNKEL, LM
    BRUNS, G
    MORLE, F
    KOENIG, M
    MANDEL, JL
    HORWICH, A
    LATT, SA
    GUSELLA, JF
    HOUSMAN, D
    FRANCKE, U
    AMERICAN JOURNAL OF HUMAN GENETICS, 1985, 37 (02) : 235 - 249
  • [35] Contiguous Xp21 deletion involving Duchenne muscular dystrophy and McLeod neuroacanthocytosis syndrome results in rapidly progressive and fatal cardiomyopathy
    Blackstone, William Z.
    Malaguit, Seth E.
    Shwaish, Natalie S.
    Frandsen, Erik L.
    CARDIOLOGY IN THE YOUNG, 2025,
  • [36] PRENATAL-DIAGNOSIS OF DUCHENNE MUSCULAR-DYSTROPHY BASED ON XP21.2 DELETION
    IONASESCU, VV
    SEARBY, C
    IONASESCU, R
    NEUROLOGY, 1986, 36 (08) : 1143 - 1144
  • [37] DELETION SCREENING IN PATIENTS WITH DUCHENNE MUSCULAR-DYSTROPHY
    WULFF, K
    HERRMANN, FH
    WAPENAAR, MC
    WEHNERT, M
    JOURNAL OF NEUROLOGY, 1989, 236 (08) : 470 - 473
  • [38] MOLECULAR DELETION ANALYSIS IN DUCHENNE MUSCULAR-DYSTROPHY
    THOMAS, NST
    RAY, PN
    WORTON, RG
    HARPER, PS
    JOURNAL OF MEDICAL GENETICS, 1986, 23 (06) : 509 - 515
  • [39] Xp21/A Translocation: A Rarely Considered Genetic Cause for Manifesting Carriers of Duchenne Muscular Dystrophy
    Trippe, Heike
    Wieczorek, Stefan
    Koetting, Judith
    Kress, Wolfram
    Schara, Ulrike
    NEUROPEDIATRICS, 2014, 45 (05) : 333 - 335
  • [40] DELETION ANALYSIS FOR DUCHENNE (AND BECKER) MUSCULAR-DYSTROPHY
    KIMBER, RD
    HYLAND, VJ
    HAAN, EA
    MULLEY, JC
    AUSTRALIAN PAEDIATRIC JOURNAL, 1989, 25 (05): : 292 - 295