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Volumn 4, Issue , 1998, Pages 31-
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Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin gene.
a a a a a a a a a a a a a a a a a a a a more.. |
Author keywords
[No Author keywords available]
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Indexed keywords
LACTOFERRIN;
AMYLOIDOSIS;
ARTICLE;
CHROMOSOME 3;
CHROMOSOME MAP;
CONGENITAL CORNEA DYSTROPHY;
FEMALE;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENETIC LINKAGE;
GENETIC POLYMORPHISM;
GENETICS;
HAPLOTYPE;
HUMAN;
MALE;
PEDIGREE;
SINGLE STRAND CONFORMATION POLYMORPHISM;
AMYLOIDOSIS;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 3;
CORNEAL DYSTROPHIES, HEREDITARY;
FEMALE;
HAPLOTYPES;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
LACTOFERRIN;
LINKAGE (GENETICS);
MALE;
PEDIGREE;
POLYMORPHISM, GENETIC;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
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EID: 17944397416
PISSN: None
EISSN: 10900535
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (33)
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References (0)
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