Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma

Cancer Letters

Volumn 228, Issue 1-2, 2005, Pages 51-58

  Bourdeaut, Franck ^a   Trochet, Delphine ^b   Janoueix Lerosey, Isabelle ^a   Ribeiro, Agnès ^a   Deville, Anne ^c   Coz, Carole ^d   Michiels, Jean François ^e   Lyonnet, Stanislas ^b   Amiel, Jeanne ^b   Delattre, Olivier ^a  

^a INSTITUT CURIE   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c Hospital Lanval   (France)

^d TIMONE HOSPITAL   (France)

^e PASTEUR HOSPITAL   (France)

Author keywords

Hirschsprung disease; Neuroblastoma; PHOX2B

Indexed keywords

HOMEOBOX PROTEIN PHOX2B; HOMEODOMAIN PROTEIN; UNCLASSIFIED DRUG;

CANCER GENETICS; CARCINOGENESIS; FAMILY; GANGLIONEUROMA; GENE LOCUS; GENE MUTATION; HEREDITY; HETEROZYGOSITY LOSS; HIRSCHSPRUNG DISEASE; HUMAN; INFANCY; NERVOUS SYSTEM DEVELOPMENT; NEUROBLASTOMA; NONHUMAN; ONCOLOGY; PEDIATRICS; PRIORITY JOURNAL; RELATIVE; SHORT SURVEY; SIBLING;

EID: 23944491142     PISSN: 03043835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.canlet.2005.01.055     Document Type: Review

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