Association between osteosarcoma and deleterious mutations in the RECQL4 gene Rothmund-Thomson syndrome

Journal of the National Cancer Institute

Volumn 95, Issue 9, 2003, Pages 669-674

  Wang, Lisa L ^a   Gannavarapu, Anu ^a   Kozinetz, Claudia A ^a   Levy, Moise L ^a   Lewis, Richard A ^a   Chintagumpala, Murali M ^a   Ruiz Maldanado, Ramon ^b   Contreras Ruiz, Jose ^c   Cunniff, Christopher ^d   Erickson, Robert P ^d   Lev, Dorit ^e   Rogers, Maureen ^f   Zackai, Elaine H ^g   Plon, Sharon E ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^c Hospital General Dr MG Gonzalez   (Mexico)

^d UNIVERSITY OF ARIZONA COLLEGE OF MEDICINE   (United States)

^e WOLFSON MEDICAL CENTER   (Israel)

^f CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^g UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; HELICASE; PROTEIN RECQL4; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; CANCER INCIDENCE; CANCER RISK; CANCER SURVIVAL; CHILD; CLINICAL ARTICLE; CLINICAL OBSERVATION; COHORT ANALYSIS; CONTROLLED STUDY; DIAGNOSTIC PROCEDURE; DISEASE ASSOCIATION; EXON; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC PREDISPOSITION; HETEROZYGOTE; HIGH RISK PATIENT; HUMAN; HUMAN CELL; HUMAN TISSUE; INTRON; KAPLAN MEIER METHOD; MALE; NUCLEOTIDE SEQUENCE; OSTEOSARCOMA; PATIENT INFORMATION; PREDICTION; PRIORITY JOURNAL; PROTEIN FUNCTION; RISK ASSESSMENT; ROTHMUND THOMSON SYNDROME; SEQUENCE ANALYSIS; STATISTICAL ANALYSIS;

EID: 0038288850     PISSN: 00278874     EISSN: None     Source Type: Journal    
DOI: 10.1093/jnci/95.9.669     Document Type: Article

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