EFFECT ON SPLICING OF A SILENT FGFR2 MUTATION IN CROUZON SYNDROME

被引：73

作者：

LI, X

PARK, WJ

PYERITZ, RE

JABS, EW

机构：

[1] JOHNS HOPKINS UNIV,SCH MED,DEPT MED,BALTIMORE,MD 21287

[2] JOHNS HOPKINS UNIV,SCH MED,DEPT SURG,BALTIMORE,MD 21287

[3] ALLEGHENY SINGER RES INST,DEPT MED GENET,PITTSBURGH,PA 15212

来源：

NATURE GENETICS | 1995年 / 9卷 / 03期

关键词：

D O I：

10.1038/ng0395-232

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

收藏

页码：232 / 233

页数：2

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[1] JACKSON-WEISS-SYNDROME AND CROUZON-SYNDROME ARE ALLELIC WITH MUTATIONS IN FIBROBLAST GROWTH-FACTOR RECEPTOR-2
JABS, EW
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MAO, JI
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[J]. NATURE GENETICS, 1994, 8 (03) : 275 - 279
[2] CRANIOFACIAL SYNDROMES - NO SUCH THING AS A SINGLE-GENE DISEASE
MULVIHILL, JT
[J]. NATURE GENETICS, 1995, 9 (02) : 101 - 103
[3] MUTATIONS IN THE FIBROBLAST GROWTH-FACTOR RECEPTOR-2 GENE CAUSE CROUZON-SYNDROME
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[J]. NATURE GENETICS, 1994, 8 (01) : 98 - 103
[4] RNA SPLICE JUNCTIONS OF DIFFERENT CLASSES OF EUKARYOTES - SEQUENCE STATISTICS AND FUNCTIONAL IMPLICATIONS IN GENE-EXPRESSION
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