Prenatal DNA diagnosis of a single-gene disorder from maternal plasma
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference4 articles.
1. Prenatal diagnosis of ornitine transcarbamylase deficiency by using a single nucleated erythrocyte from maternal blood;Watanabe;Hum Genet,1998
2. Presence of fetal DNA in maternal plasma and serum;Lo;Lancet,1997
3. Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma;Lo;N Engl J Med,1998
4. Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia;Shiang;Cell,1994
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