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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1996-2-1
|
| pubmed:abstractText |
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.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Oct
|
| pubmed:issn |
0268-3369
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
16
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
625-6
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:8528183-Adult,
pubmed-meshheading:8528183-Bone Marrow Transplantation,
pubmed-meshheading:8528183-Female,
pubmed-meshheading:8528183-Fragile X Syndrome,
pubmed-meshheading:8528183-Humans,
pubmed-meshheading:8528183-Male,
pubmed-meshheading:8528183-Tissue Donors,
pubmed-meshheading:8528183-Transplantation, Homologous,
pubmed-meshheading:8528183-X Chromosome
|
| pubmed:year |
1995
|
| pubmed:articleTitle |
Allogeneic BMT from a donor with fragile X syndrome: cytogenetic and molecular evaluation.
|
| pubmed:affiliation |
Department of Haematology and Bone Marrow Transplantation, Royal Brisbane Hospital, Herston, Queensland, Australia.
|
| pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|