Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonography
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine
Reference9 articles.
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2. Beckwith-Wiedemann syndrome: imprinting in clusters revisited;Maher;J Clin Invest,2000
3. Detailed analysis of the methylation patterns of the KvDMR1 imprinting control region of human chromosome 11;Beatty;Genomics,2006
4. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome;Gaston;Eur J Hum Genet,2001
5. Epigenotype–phenotype correlations in Beckwith-Wiedemann syndrome;Engel;J Med Genet,2000
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2. DNA Framework-Supported Electrochemical Analysis of DNA Methylation for Prostate Cancers;Nano Letters;2020-08-28
3. Prenatal diagnosis of paternal duplication of 11p15.5→14.3: Its implication of Beckwith–Wiedemann syndrome;Taiwanese Journal of Obstetrics and Gynecology;2016-12
4. Molecular Genetics and Prenatal Diagnosis;Genetic Disorders and the Fetus;2010-09-24
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