Neurofibromatosis type 1: a common familial cancer syndrome.

Methods in molecular medicine

Volumn 92, Issue , 2004, Pages 285-310

  Upadhyaya, Meena ^a   Thompson, Peter ^a   Han, Song ^a   Cooper, David N ^a  

^a UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; MOLECULAR PROBE; MUTATION; NEOPLASM; NEUROFIBROMATOSIS; SYNDROME; TUMOR SUPPRESSOR GENE;

CHROMATOGRAPHY, HIGH PRESSURE LIQUID; GENES, NEUROFIBROMATOSIS 1; GENES, TUMOR SUPPRESSOR; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MOLECULAR PROBES; MUTATION; NEOPLASMS; NEUROFIBROMATOSIS 1; SYNDROME;

EID: 1842831174     PISSN: 15431894     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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