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Volumn 25, Issue 8 SUPPL., 2005, Pages
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Challenges in genetic testing for clinical trials of inherited and orphan retinal diseases
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Author keywords
[No Author keywords available]
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Indexed keywords
ALLELE;
AUTOSOMAL RECESSIVE DISORDER;
CONFERENCE PAPER;
DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
DNA SEQUENCE;
GENE IDENTIFICATION;
GENE MUTATION;
GENETIC ANALYSIS;
GENETIC HETEROGENEITY;
GENETIC PROCEDURES;
GENETIC SCREENING;
GENETIC VARIABILITY;
GENOTYPE;
HUMAN;
LEBER CONGENITAL AMAUROSIS;
METHODOLOGY;
RETINA DEGENERATION;
RETINA DISEASE;
RETINITIS PIGMENTOSA;
SINGLE NUCLEOTIDE POLYMORPHISM;
SINGLE STRAND CONFORMATION POLYMORPHISM;
CLINICAL TRIAL;
DIAGNOSTIC PROCEDURE;
ECONOMICS;
EYE DISEASE;
GENETICS;
RARE DISEASE;
REVIEW;
CLINICAL TRIALS;
EYE DISEASES, HEREDITARY;
GENETIC SCREENING;
HUMANS;
MOLECULAR DIAGNOSTIC TECHNIQUES;
RARE DISEASES;
RETINAL DISEASES;
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EID: 33644876004
PISSN: 0275004X
EISSN: None
Source Type: Journal
DOI: 10.1097/00006982-200512001-00034 Document Type: Conference Paper |
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Times cited : (6)
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References (0)
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