| Allogeneic BMT from a donor with fragile X syndrome: cytogenetic and molecular evaluation. | |
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MedLine Citation:
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PMID: 8528183 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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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. |
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Authors:
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J Morton; L Arnold; B Fletcher; C McCarthy; J Rowell; S Durrant |
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Publication Detail:
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Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: Bone marrow transplantation Volume: 16 ISSN: 0268-3369 ISO Abbreviation: Bone Marrow Transplant. Publication Date: 1995 Oct |
Date Detail:
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Created Date: 1996-02-01 Completed Date: 1996-02-01 Revised Date: 2006-11-15 |
Medline Journal Info:
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Nlm Unique ID: 8702459 Medline TA: Bone Marrow Transplant Country: ENGLAND |
Other Details:
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Languages: eng Pagination: 625-6 Citation Subset: IM |
Affiliation:
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Department of Haematology and Bone Marrow Transplantation, Royal Brisbane Hospital, Herston, Queensland, Australia. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Adult Bone Marrow Transplantation* Female Fragile X Syndrome / genetics* Humans Male Tissue Donors Transplantation, Homologous X Chromosome |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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