Large plexiform neurofibromas may be explained as a type 2 segmental manifestation of neurofibromatosis 1 [2]

American Journal of Medical Genetics

Volumn 98, Issue 4, 2001, Pages 363-364

  Happle, Rudolf ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME MOSAICISM; EMBRYO DEVELOPMENT; HETEROZYGOSITY LOSS; LETTER; NEUROFIBROMA; NEUROFIBROMATOSIS; PRIORITY JOURNAL;

GENES, NEUROFIBROMATOSIS 1; HUMANS; LOSS OF HETEROZYGOSITY; NEUROFIBROMA, PLEXIFORM; NEUROFIBROMATOSIS 1; PERIPHERAL NERVOUS SYSTEM DISEASES;

EID: 0035253787     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20010201)98:4<363::AID-AJMG1101>3.0.CO;2-A     Document Type: Letter

References (21)

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3. Intracranial abnormalities associated with facial plexiform neurofibromas in neurofibromatosis type 1
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5. Clonal origin of tumor cells in a plexiform neurofibroma with LOH in NF 1 intron 38 and in dermal neurofibromas without LOH of the NF1 gene
6. Toward a survey of somatic mutation of the NF 1 gene in benign neurofibromas of patients with neurofibromatosis type 1
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16. Allelic loss in the NF1 gene in NF1-associated plexiform neurofibromas
17. Plexiform neurofibromas
18. Plexiform neurofibroma with and without associated malignant peripheral nerve sheath tumor: A clinicopathologic and immunohistochemical analysis of 54 cases
19. The neurofibromatoses
20. Genetic and cellular defects contributing to benign tumor formation in neurofibromatosis type 1