CLONING AND CHARACTERIZATION OF FIBRILLIN CDNA, A CANDIDATE GENE FOR THE MARFAN-SYNDROME

被引:0
|
作者
MASLEN, CL
CORSON, GM
SAKAI, LY
机构
[1] SHRINERS HOSP CRIPPLED CHILDREN,PORTLAND,OR
[2] OREGON HLTH SCI UNIV,PORTLAND,OR 97201
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:20 / 20
页数:1
相关论文
共 50 条
  • [1] CLONING AND ANALYSIS OF THE CANDIDATE FIBRILLIN GENE FOR MARFAN-SYNDROME
    LEE, B
    VITALE, E
    RAMIREZ, F
    MATTEI, MG
    GODFREY, M
    HOLLISTER, D
    AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 20 - 20
  • [2] MUTATIONS IN THE FIBRILLIN GENE AND VARIABILITY OF THE MARFAN-SYNDROME
    DIETZ, HC
    PYERITZ, RE
    CUTTING, GR
    FRANCOMANO, CA
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1992, 24 : S76 - S76
  • [3] THE MARFAN-SYNDROME IS CAUSED BY A POINT MUTATION IN THE FIBRILLIN GENE
    MAUMENEE, IH
    ARCHIVES OF OPHTHALMOLOGY, 1992, 110 (04) : 472 - 473
  • [4] PARTIAL SEQUENCE OF A CANDIDATE GENE FOR THE MARFAN-SYNDROME
    MASLEN, CL
    CORSON, GM
    MADDOX, BK
    GLANVILLE, RW
    SAKAI, LY
    NATURE, 1991, 352 (6333) : 334 - 337
  • [5] ABNORMAL FIBRILLIN METABOLISM IN BOVINE MARFAN-SYNDROME
    POTTER, KA
    HOFFMAN, Y
    SAKAI, LY
    BYERS, PH
    BESSER, TE
    MILEWICZ, DM
    AMERICAN JOURNAL OF PATHOLOGY, 1993, 142 (03): : 803 - 810
  • [6] MARFAN-SYNDROME CAUSED BY A RECURRENT DENOVO MISSENSE MUTATION IN THE FIBRILLIN GENE
    DIETZ, HC
    CUTTING, GR
    PYERITZ, RE
    MASLEN, CL
    SAKAI, LY
    CORSON, GM
    PUFFENBERGER, EG
    HAMOSH, A
    NANTHAKUMAR, EJ
    CURRISTIN, SM
    STETTEN, G
    MEYERS, DA
    FRANCOMANO, CA
    NATURE, 1991, 352 (6333) : 337 - 339
  • [7] DIFFERENTIAL ALLELIC EXPRESSION OF A FIBRILLIN GENE (FBNI) IN PATIENTS WITH MARFAN-SYNDROME
    HEWETT, D
    LYNCH, J
    CHILD, A
    FIRTH, H
    SYKES, B
    AMERICAN JOURNAL OF HUMAN GENETICS, 1994, 55 (03) : 447 - 452
  • [8] A NEW MISSENSE MUTATION OF FIBRILLIN IN A PATIENT WITH MARFAN-SYNDROME
    HEWETT, DR
    LYNCH, JR
    CHILD, A
    SYKES, BC
    JOURNAL OF MEDICAL GENETICS, 1994, 31 (04) : 338 - 339
  • [9] MUTATIONS IN THE FIBRILLIN GENE RESPONSIBLE FOR DOMINANT ECTOPIA LENTIS AND NEONATAL MARFAN-SYNDROME
    KAINULAINEN, K
    KARTTUNEN, L
    PUHAKKA, L
    SAKAI, L
    PELTONEN, L
    NATURE GENETICS, 1994, 6 (01) : 64 - 69
  • [10] SCREENING OF MARFAN-SYNDROME PATIENTS FOR MUTATIONS IN THE FIBRILLIN (FBN1) GENE
    HAYWARD, C
    LOGIE, LJ
    PORTEOUS, MEM
    BROCK, DJH
    JOURNAL OF MEDICAL GENETICS, 1995, 32 (02) : 137 - 137