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dc.contributor.authorAktas, D
dc.contributor.authorYenicesu, I
dc.contributor.authorHicsonmez, G
dc.contributor.authorTuncbilek, E
dc.date.accessioned2019-12-10T10:40:01Z
dc.date.available2019-12-10T10:40:01Z
dc.date.issued1999
dc.identifier.issn0361-8609
dc.identifier.urihttps://doi.org/10.1002/(SICI)1096-8652(199909)62:1<49::AID-AJH8>3.3.CO;2-P
dc.identifier.urihttp://hdl.handle.net/11655/14137
dc.description.abstractMonosomy 7 or partial deletion of the long arm of chromosome 7 is frequently described in children with myelodysplastic syndrome and acute myeloblastic leukemia, Parental origin of chromosome 7 in children with sporadic monosomy 7 has been examined very rarely, To investigate if monosomy 7 shows parent-of-origin, we have studied a female child with monosomy 7 and de novo myelodysplastic syndrome by a series of polymorphic polymerase chain reaction markers. We found loss of maternal allele and discussed the results with the previous reports. Am, J, Hematol. 62:49-51, 1999. (C) 1999 Wiley-Liss, Inc.
dc.language.isoen
dc.publisherWiley-Liss
dc.relation.isversionof10.1002/(SICI)1096-8652(199909)62:1<49::AID-AJH8>3.3.CO;2-P
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectHematology
dc.titleLoss of Maternal Allele in a Child with Myelodysplastic Syndrome and Monosomy 7
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalAmerican Journal Of Hematology
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume62
dc.identifier.issue1
dc.identifier.startpage49
dc.identifier.endpage51
dc.description.indexWoS


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