Spectrum of RB1 gene mutations and loss of heterozygosity in Mexican patients with retinoblastoma: Identification of six novel mutations

Cancer Biomarkers

Volumn 4, Issue 2, 2008, Pages 93-99

  Macias M ^a,b   Dean, M ^c   Atkinson, A ^c   Jimenez Morales S ^d   Garcia Vazquez F J ^a   Saldana Alvarez Y ^d   Ramirez Bello J ^d   Chavez M ^a   Orozco, L ^d  

^a INSTITUTO NACIONAL DE PEDIATRÍA   (Mexico)

^b UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^c NATIONAL CANCER INSTITUTE   (United States)

^d INSTITUTO NACIONAL DE MEDICINA GENÓMICA   (Mexico)

Author keywords

Loss of heterozygosity; Mexican patients; Mutations; RB1 gene; Retinoblastoma

Indexed keywords

ADENINE; CYTOSINE; GUANINE; RETINOBLASTOMA PROTEIN; RETINOBLASTOMA PROTEIN 1; THYMINE;

ARTICLE; CANCER DIAGNOSIS; CARCINOGENESIS; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE IDENTIFICATION; GENE INACTIVATION; GENE SEQUENCE; GENETIC COUNSELING; GENETIC RISK; GENETIC SCREENING; GENETIC VARIABILITY; HETEROZYGOSITY LOSS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INFANT; INTRON; MALE; MEXICO; MOLECULAR MECHANICS; MUTATIONAL ANALYSIS; NONSENSE MUTATION; NUCLEIC ACID BASE SUBSTITUTION; ONSET AGE; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINOBLASTOMA; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 44049088579     PISSN: 15740153     EISSN: None     Source Type: Journal    
DOI: 10.3233/CBM-2008-4205     Document Type: Article

References (58)