Cryptic deletions and inversions of chromosome 21 in a phenotypically normal infant with transient abnormal myelopoiesis: a molecular cytogenetic study
Open Access
- 1 November 1998
- journal article
- case report
- Published by Wiley in British Journal of Haematology
- Vol. 103 (2) , 473-479
- https://doi.org/10.1046/j.1365-2141.1998.00996.x
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Deletions of chromosome 21 restricted to the leukemic cells of children with Down syndrome and leukemiaLeukemia, 1997
- Clonal Hematologic Disorders in Down Syndrome A ReviewJournal of Pediatric Hematology/Oncology, 1995
- Cloning and Characterization of a 135- to 500-kb Region of Homology on the Long Arm of Human Chromosome 21Genomics, 1994