Syndrome-related chromosome-specific radiation-induced break points of various inherited human metabolic disorders

Mutation Research - Genetic Toxicology and Environmental Mutagenesis

Volumn 538, Issue 1-2, 2003, Pages 133-143

  Radha, S ^a,b   Marimuthu, K M ^a  

^a UNIVERSITY OF MADRAS   (India)

^b VIT UNIVERSITY   (India)

Author keywords

Chromosomal radiosensitivity; Cytogenetics of metabolic disorders

Indexed keywords

DNA;

ADULT; ALPHA THALASSEMIA; ARTICLE; CHILD; CHROMOSOME 1; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CLINICAL ARTICLE; CONTROLLED STUDY; DENSITOMETRY; DISEASE ASSOCIATION; DNA CONTENT; DNA PROBE; DUCHENNE MUSCULAR DYSTROPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GAMMA RADIATION; GENE LOCUS; HEMOPHILIA; HUMAN; ICHTHYOSIS; INHERITANCE; IRRADIATION; LYMPHOCYTE CULTURE; METABOLIC DISORDER; PRIORITY JOURNAL; RADIATION DOSE; RETINITIS PIGMENTOSA; Y CHROMOSOME;

EID: 0038433244     PISSN: 13835718     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1383-5718(03)00111-6     Document Type: Article

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