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Volumn 14, Issue 4, 1996, Pages 479-481
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Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13
a a a a a a a a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
ARTICLE;
CHROMOSOMAL LOCALIZATION;
CHROMOSOME 20P;
FEMALE;
GENE MAPPING;
HALLERVORDEN SPATZ DISEASE;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
PRIORITY JOURNAL;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 20;
CONSANGUINITY;
FEMALE;
GENETIC MARKERS;
HALLERVORDEN-SPATZ SYNDROME;
HOMOZYGOTE;
HUMANS;
LINKAGE (GENETICS);
MALE;
PEDIGREE;
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EID: 16144365391
PISSN: 10614036
EISSN: None
Source Type: Journal
DOI: 10.1038/ng1296-479 Document Type: Article |
Times cited : (142)
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References (0)
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