FREQUENCY OF DELTA-F508 MUTATION AND HAPLOTYPE ANALYSIS IN AUSTRIAN CYSTIC-FIBROSIS FAMILIES

被引：0
|
作者：
LARSEN, J
GEORGHIOU, A
KURY, FD
GOTZ, M
SANZ, K
DOBIANER, K
SPONA, J
机构：
[1] LUDWIG BOLTZMANN INST EXPTL ENDOKRINOL,ZELLULARE ENDOKRINOL ABT,SPITALGASSE 23,A-1090 VIENNA,AUSTRIA
[2] UNIV VIENNA,KINDERKLIN,A-1010 VIENNA,AUSTRIA
[3] ERSTE UNIV WIEN,FRAUEN KLIN,VIENNA,AUSTRIA
来源：
HUMAN GENETICS | 1992年 / 89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：
引用
收藏
页码：464 / 465
页数：2
相关论文
共 50 条
  • [31] CLINICAL CHARACTERIZATION OF CYSTIC-FIBROSIS PATIENTS CARRYING THE DELTA-F508 MUTATION
    KEREM, E
    KEREM, BS
    COREY, M
    ROMMENS, J
    LEVISON, H
    TSUI, LC
    DURIE, P
    PEDIATRIC RESEARCH, 1990, 27 (04) : A358 - A358
  • [32] THE ORIGIN OF THE MAJOR CYSTIC-FIBROSIS MUTATION (DELTA-F508) IN EUROPEAN POPULATIONS
    MORRAL, N
    BERTRANPETIT, J
    ESTIVILL, X
    NUNES, V
    CASALS, T
    GIMENEZ, J
    REIS, A
    VARONMATEEVA, R
    MACEK, M
    KALAYDJIEVA, L
    ANGELICHEVA, D
    DANCHEVA, R
    ROMEO, G
    RUSSO, MP
    GARNERONE, S
    RESTAGNO, G
    FERRARI, M
    MAGNANI, C
    CLAUSTRES, M
    DESGEORGES, M
    SCHWARTZ, M
    SCHWARZ, M
    DALLAPICCOLA, B
    NOVELLI, G
    FEREC, C
    DEARCE, M
    NEMETI, M
    KERE, T
    ANVRET, M
    DAHL, N
    KADASI, L
    NATURE GENETICS, 1994, 7 (02) : 169 - 175
  • [33] A POOLING STRATEGY FOR HETEROZYGOTE SCREENING OF THE DELTA-F508 CYSTIC-FIBROSIS MUTATION
    GILLE, C
    GRADE, K
    COUTELLE, C
    HUMAN GENETICS, 1991, 86 (03) : 289 - 291
  • [34] CYSTIC-FIBROSIS MUTATION DELTA-F508 IN FINLAND - OTHER MUTATIONS PREDOMINATE
    KERE, J
    SAVILAHTI, E
    NORIO, R
    ESTIVILL, X
    DELACHAPELLE, A
    HUMAN GENETICS, 1990, 85 (04) : 413 - 415
  • [35] SEVERITY OF CYSTIC-FIBROSIS IN PATIENTS HOMOZYGOUS AND HETEROZYGOUS FOR DELTA-F508 MUTATION
    JOHANSEN, HK
    NIR, M
    HOIBY, N
    KOCH, C
    SCHWARTZ, M
    LANCET, 1991, 337 (8742): : 631 - 634
  • [36] ENDOCRINE AND EXOCRINE PANCREATIC FUNCTION AND THE DELTA-F508 MUTATION IN CYSTIC-FIBROSIS
    LANNG, S
    SCHWARTZ, M
    THORSTEINSSON, B
    KOCH, C
    CLINICAL GENETICS, 1991, 40 (05) : 345 - 348
  • [37] DNA DIAGNOSIS OF CYSTIC-FIBROSIS BY DIRECT DETECTION OF THE DELTA-F508 MUTATION
    HENDRICKX, J
    WAUTERS, J
    COUCKE, P
    VITS, L
    VANDERAUWERA, B
    WILLEMS, PJ
    ACTA CLINICA BELGICA, 1991, 46 (01): : 13 - 17
  • [38] PRENATAL SCREENING FOR DELTA-F508 MUTATION IN POPULATION NOT SELECTED FOR CYSTIC-FIBROSIS
    BICK, D
    BLACK, SH
    CUMMINGS, E
    COSTAKOS, D
    MADDALENA, A
    HEADRICK, EG
    JONES, SL
    BECKER, R
    SCHULMAN, JD
    LANCET, 1990, 336 (8726): : 1324 - 1325
  • [39] PRENATAL PREDICTION OF CYSTIC-FIBROSIS IN A MOTHER HOMOZYGOUS FOR THE DELTA-F508 MUTATION
    DAHL, N
    KOLLBERG, H
    CLINICAL GENETICS, 1992, 42 (04) : 214 - 215
  • [40] PRELIMINARY-RESULTS ON THE FREQUENCY OF THE DELTA-F508 MUTATION IN CYSTIC-FIBROSIS PATIENTS FROM THE USSR
    RONCHETTO, P
    DEVOTO, M
    PULITI, A
    ROMEO, G
    SOKOLOV, B
    KALININ, VN
    VORSANOVA, SG
    KRAINIAIA, GV
    REZNIK, BY
    HUMAN GENETICS, 1990, 85 (04) : 423 - 424
12345