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A case of retinoblastoma, associated with histiocytosis‐X and mosaicism of a deleted D‐group chromosome (13q14→q31)
Author(s) -
Orye E.,
Benoit Y.,
Coppieters R.,
Jeannin Ph.,
Vercruysse C.,
Delaey J.,
Delbeke M.J.
Publication year - 1982
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1982.tb01408.x
Subject(s) - retinoblastoma , biology , chromosome , genetics , mitosis , chromosome 13 , gene
A previously unpublished association of retinoblastoma and histiocytosis‐X is described in a girl. In addition, chromosome analysis revealed a mosaicism of normal and abnormal mitoses. A deleted D‐group chromosome (13q14‐q31) was present.

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