Lineage-specific trisomy 21 in a neonate with resolving transient myeloproliferative syndrome. [electronic resource]
Producer: 20020523Description: 224-6 p. digitalISSN:- 1077-4114
- Adult
- Antigens, CD -- metabolism
- Cell Lineage -- genetics
- Chromosomes, Human, Pair 21 -- genetics
- Down Syndrome -- genetics
- Erythrocytes
- Female
- Hematopoietic Stem Cells
- Humans
- In Situ Hybridization, Fluorescence
- Infant, Newborn
- Karyotyping
- Monocytes
- Mosaicism -- genetics
- Myeloproliferative Disorders -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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