REPEAT POLYMORPHISMS IN HUMAN FIBRILLIN GENES ON CHROMOSOME-15 (FBN1) AND CHROMOSOME-5 (FBN2)

被引:4
作者
BIDDINGER, AL
HECHT, JT
MILEWICZ, DM
机构
[1] UNIV TEXAS,SCH MED,DEPT MED,6431 FANNIN,HOUSTON,TX 77030
[2] UNIV TEXAS,SCH MED,DEPT PEDIAT,HOUSTON,TX 77030
关键词
D O I
10.1093/hmg/2.8.1323
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:1323 / 1323
页数:1
相关论文
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  • [2] LINKAGE OF MARFAN-SYNDROME AND A PHENOTYPICALLY RELATED DISORDER TO 2 DIFFERENT FIBRILLIN GENES
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    HORI, H
    MATTEI, MG
    SARFARAZI, M
    TSIPOURAS, P
    RAMIREZ, F
    HOLLISTER, DW
    [J]. NATURE, 1991, 352 (6333) : 330 - 334
  • [3] PYERITZ, 1977, NEW ENGL J MED, V300, P772