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Volumn 21, Issue 3, 2001, Pages 202-206
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Prenatal diagnosis of hereditary spastic paraplegia
d
NONE
(United States)
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Author keywords
Paraplegia; Spasticity; Strumpell Lorrain
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Indexed keywords
MICROSATELLITE DNA;
ADULT;
ALLELE;
ARTICLE;
AUTOSOMAL DOMINANT DISORDER;
CHORION VILLUS SAMPLING;
CHROMOSOME 10Q;
CHROMOSOME 12Q;
CHROMOSOME 14Q;
CHROMOSOME 15Q;
CHROMOSOME 19Q;
CHROMOSOME 2P;
CHROMOSOME 2Q;
CHROMOSOME 8Q;
DNA FLANKING REGION;
DNA POLYMORPHISM;
FEMALE;
GENE LOCUS;
HAPLOTYPE;
HUMAN;
PRENATAL DIAGNOSIS;
PRIORITY JOURNAL;
SPASTIC PARAPLEGIA;
ADULT;
CHROMOSOMES, HUMAN, PAIR 14;
FEMALE;
HUMANS;
MALE;
PEDIGREE;
POLYMORPHISM, GENETIC;
PREGNANCY;
PRENATAL DIAGNOSIS;
SPASTIC PARAPLEGIA, HEREDITARY;
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EID: 0035056728
PISSN: 01973851
EISSN: None
Source Type: Journal
DOI: 10.1002/1097-0223(200103)21:3<202::AID-PD4>3.0.CO;2-U Document Type: Article |
Times cited : (7)
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References (20)
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