Detection of chromosomal abnormalities in the dysmorphic fetus using fluorescence in situ hybridization: Evaluation for monosomy X genotype
- 1 November 1995
- journal article
- Published by Elsevier in Human Pathology
- Vol. 26 (11) , 1241-1244
- https://doi.org/10.1016/0046-8177(95)90200-7
Abstract
No abstract availableKeywords
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