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Allogeneic BMT from a donor with fragile X syndrome: cytogenetic and molecular evaluation
J Morton1, L Arnold, B Fletcher
1Department of Haematology and Bone Marrow Transplantation, Royal Brisbane Hospital, Herston, Queensland, Australia.
Bone Marrow Transplantation
|October 1, 1995
Abstract:
We report the first case of engraftment of bone marrow collected from a donor with Fragile X syndrome with subsequent cytogenetic and molecular evaluation. Engraftment was prompt and stable. Whilst the Fragile X abnormality could be detected initially by molecular techniques in the peripheral blood, it could not be detected cytogenetically while the patient was receiving CsA.