A STOP CODON IN A PATIENT WITH SEVERE TYPE-III VONWILLEBRAND DISEASE

被引:31
作者
BAHNAK, BR
LAVERGNE, JM
ROTHSCHILD, C
MEYER, D
机构
关键词
D O I
10.1182/blood.V78.4.1148.bloodjournal7841148
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:1148 / 1149
页数:2
相关论文
共 6 条
  • [1] RESTRICTION SITES CONTAINING CPG SHOW A HIGHER FREQUENCY OF POLYMORPHISM IN HUMAN DNA
    BARKER, D
    SCHAFER, M
    WHITE, R
    [J]. CELL, 1984, 36 (01) : 131 - 138
  • [2] HOMOZYGOUS AND HETEROZYGOUS DELETIONS OF THE VONWILLEBRAND-FACTOR GENE IN PATIENTS AND CARRIERS OF SEVERE VONWILLEBRAND DISEASE
    NGO, KY
    GLOTZ, VT
    KOZIOL, JA
    LYNCH, DC
    GITSCHIER, J
    RANIERI, P
    CIAVARELLA, N
    RUGGERI, ZM
    ZIMMERMAN, TS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (08) : 2753 - 2757
  • [3] NICHOLS WC, 1990, BLOOD S, V76, pA431
  • [4] PEAKE IR, 1990, BLOOD, V75, P654
  • [5] ENZYMATIC AMPLIFICATION OF BETA-GLOBIN GENOMIC SEQUENCES AND RESTRICTION SITE ANALYSIS FOR DIAGNOSIS OF SICKLE-CELL ANEMIA
    SAIKI, RK
    SCHARF, S
    FALOONA, F
    MULLIS, KB
    HORN, GT
    ERLICH, HA
    ARNHEIM, N
    [J]. SCIENCE, 1985, 230 (4732) : 1350 - 1354
  • [6] GENE DELETIONS CORRELATE WITH THE DEVELOPMENT OF ALLOANTIBODIES IN VONWILLEBRAND DISEASE
    SHELTONINLOES, BB
    CHEHAB, FF
    MANNUCCI, PM
    FEDERICI, AB
    SADLER, JE
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (05) : 1459 - 1465