A common single-nucleotide variant in T is strongly associated with chordoma

Nature Genetics

Volumn 44, Issue 11, 2012, Pages 1185-1187

  Pillay, Nischalan ^a,b   Plagnol, Vincent ^a   Tarpey, Patrick S ^c   Lobo, Samira B ^b   Presneau, Nadège ^a   Szuhai, Karoly ^d   Halai, Dina ^b   Berisha, Fitim ^b   Cannon, Stephen R ^b   Mead, Simon ^e   Kasperaviciute, Dalia ^e   Palmen, Jutta ^a   Talmud, Philippa J ^a   Kindblom, Lars Gunnar ^f   Amary, M Fernanda ^b   Tirabosco, Roberto ^b   Flanagan, Adrienne M ^a,b  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b ROYAL NATIONAL ORTHOPAEDIC HOSPITAL   (United Kingdom)

^c WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^d LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^e UNIVERSITY COLLEGE LONDON   (United Kingdom)

^f ROYAL ORTHOPAEDIC HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; TRANSCRIPTION FACTOR;

ALLELE; ARTICLE; BINDING AFFINITY; CHORDOMA; CLINICAL ARTICLE; COHORT ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; COPY NUMBER VARIATION; EMBRYONIC STEM CELL; EXOME; EXON; GENE EXPRESSION; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HUMAN; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SINGLE NUCLEOTIDE POLYMORPHISM;

BONE NEOPLASMS; CHORDOMA; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXOME; FETAL PROTEINS; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA; T-BOX DOMAIN PROTEINS;

EID: 84868213270     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.2419     Document Type: Article

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