Lineage-specific trisomy 21 in a neonate with resolving transient myeloproliferative syndrome.

Slayton, William B

Lineage-specific trisomy 21 in a neonate with resolving transient myeloproliferative syndrome. [electronic resource] - Journal of pediatric hematology/oncology - 224-6 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

1077-4114

10.1097/00043426-200203000-00013 doi


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