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Volumn 8, Issue 3, 2000, Pages
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A genetic hypothesis for Chiari I malformation with or without syringomyelia.
a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
ARNOLD CHIARI MALFORMATION;
ARTICLE;
COMPARATIVE STUDY;
FEMALE;
GENETIC PREDISPOSITION;
GENETICS;
HUMAN;
MALE;
SYRINGOMYELIA;
ARNOLD-CHIARI MALFORMATION;
FEMALE;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
MALE;
SYRINGOMYELIA;
MLCS;
MLOWN;
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EID: 33747143163
PISSN: None
EISSN: 10920684
Source Type: Journal
DOI: 10.3171/foc.2000.8.3.12 Document Type: Article |
Times cited : (85)
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References (0)
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