Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes-Reference-Cited by-同舟云学术

Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes

Published:2011-01-28 Issue:2 Volume:32 Page:249-258
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Azzi Salah,Steunou Virginie,Rousseau Alexandra,Rossignol Sylvie,Thibaud Nathalie,Danton Fabienne,Le Jule Marilyne,Gicquel Christine,Le Bouc Yves,Netchine Irène

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21403/fullpdf

Reference38 articles.

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2. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci;Azzi;Hum Mol Genet,2009

3. Statistical methods for assessing agreement between two methods of clinical measurement;Bland;Lancet,1986

4. Restriction site-specific methylation studies of imprinted genes with quantitative real-time PCR;Bruce;Clin Chem,2008

5. Molecular diagnosis of Beckwith-Wiedemann syndrome using quantitative methylation-sensitive polymerase chain reaction;Coffee;Genet Med,2006

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1. Maintenance of methylation profile in imprinting control regions in human induced pluripotent stem cells;Clinical Epigenetics;2022-12

2. Height and body mass index in molecularly confirmed Silver–Russell syndrome and the long‐term effects of growth hormone treatment;Clinical Endocrinology;2022-03-21

3. Prenatal molecular testing and diagnosis of Beckwith‐Wiedemann syndrome;Prenatal Diagnosis;2021-05-18

4. DNA methylation as an epigenetic biomarker in imprinting disorders;Postępy Higieny i Medycyny Doświadczalnej;2020-12-07

5. Preclinical and Clinical Epigenetic-Based Reconsideration of Beckwith-Wiedemann Syndrome;Frontiers in Genetics;2020-09-15