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pro vyhledávání: '"Jacqueline Challis"'
Autor:
Martin Campbell, Julie Cayrol, Yves Heloury, Michael Nightingale, Jacqueline Challis, Michael J. Sullivan
Publikováno v:
Journal of pediatric hematology/oncology. 41(8)
Background The 9q22.3 syndrome is an autosomal dominant microdeletion syndrome with similarities to Gorlin syndrome (GS). It encompasses the PTCH1 gene locus that harbors mutations for GS. Although the 9q22.3 syndrome is associated with Wilms tumor (
Publikováno v:
Cancer genetics and cytogenetics. 58(1)
A translocation involving the short arm of chromosome 2 and the long arm of chromosome 4 is described in three patients, all of whom had acute nonlymphocytic leukemia (M2). One patient had M2 de novo, one progressed from refractory anemia with excess