Constitutional and somatic RB1 mutation spectrum in nonfamilial unilateral and bilateral retinoblastoma in India

Genetic Testing

Volumn 9, Issue 3, 2005, Pages 200-211

  Bamne, M N ^a   Ghule, P N ^a   Jose, J ^a   Banavali, S D ^a   Kurkure, P A ^a   Amare, P S ^a  

^a TATA MEMORIAL HOSPITAL   (India)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; ASIA; CHILD; CHIMERA; CHROMOSOME 13Q; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; DISEASE PREDISPOSITION; EXON; EXTRACHROMOSOMAL INHERITANCE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MUTATION; HUMAN; INFANT; MALE; MOSAICISM; NEWBORN; POINT MUTATION; POLYMERASE CHAIN REACTION; PREVALENCE; RETINOBLASTOMA; RISK FACTOR; SOMATIC MUTATION; SYMPTOMATOLOGY; TUMOR SUPPRESSOR GENE;

BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; DNA PRIMERS; FEMALE; GENE DELETION; GENES, RETINOBLASTOMA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INDIA; INFANT; MALE; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RETINOBLASTOMA;

EID: 27144491919     PISSN: 10906576     EISSN: None     Source Type: Journal    
DOI: 10.1089/gte.2005.9.200     Document Type: Article

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