Acute lymphocytic leukaemia in a child with Beckwith-Wiedemann syndrome harbouring a CDKN1C mutation

European Journal of Medical Genetics

Volumn 53, Issue 6, 2010, Pages 400-403

  Abadie, C ^a   Bernard, F ^a   Netchine, I ^b,c,d   Sanlaville, D ^e,f   Roque, A ^g   Rossignol, S ^b,c,d   Coupier, I ^a,h  

^a MONTPELLIER UNIVERSITY HOSPITAL   (France)

^b ARMAND TROUSSEAU HOSPITAL   (France)

^c INSERM   (France)

^d SORBONNE UNIVERSITÉ   (France)

^e HCL   (France)

^f UNIVERSITÉ LYON 1   (France)

^g Saint Jean de Védas ^*  (France)

^h CENTRE VAL D AURELLE   (France)

Author keywords

Beckwith Wiedemann syndrome; CDKN1C; T type acute lymphoblastic leukaemia

Indexed keywords

CYCLIN DEPENDENT KINASE INHIBITOR 1C;

ACUTE LYMPHOCYTIC LEUKEMIA; ADRENAL CORTEX CARCINOMA; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CANCER RISK; CASE REPORT; CHILD; CHROMOSOME 11P; GENE CONTROL; GENE MUTATION; GENOME IMPRINTING; GENOTYPE PHENOTYPE CORRELATION; HEPATOBLASTOMA; HUMAN; MALE; NEPHROBLASTOMA; NEUROBLASTOMA; NUCLEOTIDE SEQUENCE; PHENOTYPE; RHABDOMYOSARCOMA; SCHOOL CHILD;

BECKWITH-WIEDEMANN SYNDROME; CHILD; CHROMOSOMES, HUMAN, PAIR 11; CYCLIN-DEPENDENT KINASE INHIBITOR P57; GENOMIC IMPRINTING; HUMANS; MUTATION; PRECURSOR T-CELL LYMPHOBLASTIC LEUKEMIA-LYMPHOMA;

EID: 78349312986     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2010.08.006     Document Type: Article

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