| Literature DB >> 7794514 |
G A Macones1, A Johnson, D Tilley, R Wade, R Wapner.
Abstract
The in utero diagnosis of fetal myeloproliferative disease was made by cordocentesis following the ultrasound appearance of fetal hepatosplenomegaly and mild hydrops. The 2 fetuses reported both had leukocyte counts greater than 75,000/mm3 with a predominance of blast forms. In both cases the karyotype revealed trisomy 21.Entities:
Mesh：
Year: 1995 PMID： 7794514 DOI： 10.1159/000264219
Source DB: PubMed Journal: Fetal Diagn Ther ISSN： 1015-3837 Impact factor: 2.587