14q deletions are associated with trisomy 12, NOTCH1 mutations and unmutated IGHV genes in chronic lymphocytic leukemia and small lymphocytic lymphoma

Genes Chromosomes and Cancer

Volumn 53, Issue 8, 2014, Pages 657-666

  Cosson, Adrien ^a   Chapiro, Elise ^a,b,c   Belhouachi, Nabila ^b   Cung, Hong Anh ^b   Keren, Boris ^b   Damm, Frederik ^d   Algrin, Caroline ^b   Lefebvre, Christine ^e   Fert Ferrer, Sandra ^f   Luquet, Isabelle ^g   Gachard, Nathalie ^h   Mugneret, Francine ⁱ   Terre, Christine ^j   Collonge Rame, Marie Agnes ^k   Michaux, Lucienne ^l   Rafdord Weiss, Isabelle ^m   Talmant, Pascaline ⁿ   Veronese, Lauren ^o   Nadal, Nathalie ^p   Struski, Stephanie ^q   Barin, Carole ^r   Helias, Catherine ^s   Lafage, Marina ^t   Lippert, Eric ^u   Auger, Nathalie ^d   Eclache, Virginie ^v   Roos Weil, Damien ^b,c   Leblond, Veronique ^b,c   Settegrana, Catherine ^b   Maloum, Karim ^b   Davi, Frederic ^a,b,c   Merle Beral, Helene ^a,b,c   Lesty, Claude ^b,c   Nguyen Khac, Florence ^a,b,c   more..

^a CENTRE DE RECHERCHE DES CORDELIERS   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c SORBONNE UNIVERSITÉ   (France)

^d INSTITUT GUSTAVE ROUSSY   (France)

^e GRENOBLE UNIVERSITY HOSPITAL   (France)

^f CENTRE HOSPITALIER DE CHAMBÉRY   (France)

^g REIMS UNIVERSITY HOSPITAL   (France)

^h LIMOGES UNIVERSITY HOSPITAL   (France)

ⁱ HÔPITAL DU BOCAGE   (France)

^j CENTRE HOSPITALIER DE VERSAILLES   (France)

^k UNIVERSITY HOSPITAL OF BESANÇON   (France)

^l UNIVERSITY OF LEUVEN   (Belgium)

^m HÔPITAL NECKER ENFANTS MALADES   (France)

ⁿ HÔTEL DIEU   (France)

^o UNIVERSITY HOSPITAL OF CLERMONT FERRAND   (France)

^p HÔPITAL NORD   (France)

^q CHU PURPAN   (France)

^r CHU BRETONNEAU   (France)

^s UNIVERSITY HOSPITAL OF STRASBOURG   (France)

^t INSTITUT PAOLI CALMETTES   (France)

^u BORDEAUX UNIVERSITY HOSPITAL   (France)

^v AVICENNE HOSPITAL   (France)

more..

Author keywords

[No Author keywords available]

Indexed keywords

EXPORTIN 1; IGHV PROTEIN; MYELOID DIFFERENTIATION FACTOR 88; NOTCH1 RECEPTOR; PROTEIN P53; TUMOR PROTEIN; UNCLASSIFIED DRUG; IMMUNOGLOBULIN HEAVY CHAIN; IMMUNOGLOBULIN VARIABLE REGION; NOTCH1 PROTEIN, HUMAN;

ADULT; AGED; ARTICLE; CHROMOSOME 14Q; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; CHRONIC LYMPHATIC LEUKEMIA; CONTROLLED STUDY; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; KARYOTYPE; LYMPHOCYTOMA; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; SURVIVAL; TRANSCRIPTION INITIATION; TRISOMY 12; CHROMOSOME 12; CHROMOSOME 14; GENETICS; IMMUNOGLOBULIN VARIABLE REGION; MIDDLE AGED; MUTATION; PATHOLOGY; TRISOMY; VERY ELDERLY;

ADULT; AGED; AGED, 80 AND OVER; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 14; FEMALE; HUMANS; IMMUNOGLOBULIN HEAVY CHAINS; IMMUNOGLOBULIN VARIABLE REGION; LEUKEMIA, LYMPHOCYTIC, CHRONIC, B-CELL; MALE; MIDDLE AGED; MUTATION; RECEPTOR, NOTCH1; TRISOMY;

EID: 84902152749     PISSN: 10452257     EISSN: 10982264     Source Type: Journal    
DOI: 10.1002/gcc.22176     Document Type: Article

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