MOESM4 of The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype

Sparago, Angela; Verma, Ankit; Patricelli, Maria; Pignata, Laura; Russo, Silvia; Calzari, Luciano; De Francesco, Naomi; Del Prete, Rosita; Palumbo, Orazio; Carella, Massimo; Mackay, Deborah; Rezwan, Faisal; Angelini, Claudia; Cerrato, Flavia; Cubellis, Maria; Riccio, Andrea

doi:10.6084/m9.figshare.11358122.v1

13148_2019_760_MOESM4_ESM.pdf (192.66 kB)

MOESM4 of The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype

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posted on 2019-12-12, 12:11 authored by Angela Sparago, Ankit Verma, Maria Patricelli, Laura Pignata, Silvia Russo, Luciano Calzari, Naomi De Francesco, Rosita Del Prete, Orazio Palumbo, Massimo Carella, Deborah Mackay, Faisal Rezwan, Claudia Angelini, Flavia Cerrato, Maria Cubellis, Andrea Riccio

Additional file 4: Figure S3. Examples of hypomethylated imprinted DMRs as visualized by UCSC genome browser. Each vertical line represents a CpG site. Asterisks indicate regions with discordant methylation levels in the two siblings. gDMRs: germline DMRs; sDMRs: secondary DMRs.

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Italian MIUR-PRIN

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Multi-locus imprinting disturbances NLRP5 Beckwith-Wiedemann syndrome Genomic imprinting DNA-methylation Maternal-effect variants

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MOESM4 of The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype

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