Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 gene

Cancer Genetics and Cytogenetics

Volumn 164, Issue 2, 2006, Pages 159-163

  Oguzkan, Sibel ^a   Terzi, Yunus Kasim ^b   Güler, Elif ^a   Derbent, Murat ^c   Agras, Pinar Isik ^c   Saatci, Umit ^c   Ayter, Sukriye ^b  

^a GAZIANTEP UNIVERSITY   (Turkey)

^b HACETTEPE UNIVERSITY   (Turkey)

^c BASKENT UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

NEUROFIBROMIN;

ARTICLE; BLADDER CANCER; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; DNA EXTRACTION; DNA POLYMORPHISM; FEMALE; GENE DELETION; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; HYDRONEPHROSIS; INFANT; MALE; NEUROFIBROMATOSIS; NOONAN SYNDROME; PHENOTYPE; PRIORITY JOURNAL; PYELONEPHRITIS; RHABDOMYOSARCOMA; TUMOR BIOPSY;

GENE DELETION; GENES, NEUROFIBROMATOSIS 1; GENETIC MARKERS; HUMANS; INFANT; LOSS OF HETEROZYGOSITY; MALE; NEUROFIBROMATOSIS 1; NOONAN SYNDROME; RHABDOMYOSARCOMA; URINARY BLADDER NEOPLASMS;

EID: 31144443267     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2005.08.004     Document Type: Article

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