Supplemental material
Epigenetics
Volume 7, 2012 - Issue 10
Related Research Data
The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers.
Source:
Public Library of Science (PLoS)
Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12
Source:
Springer Science and Business Media LLC
Imprinted genes, placental development and fetal growth.
Source:
S. Karger AG
Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes
Source:
Springer Science and Business Media LLC
Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2–H19 domain in bodies and placentas
Source:
Springer Science and Business Media LLC
Genomic imprinting at the mammalian Dlk1-Dio3 domain
Source:
Elsevier BV
Placentomegaly with massive hydrops of placental stem villi, diploid DNA content, and fetal omphaloceles: possible association with Beckwith-Wiedemann syndrome.
Source:
Elsevier BV
RNAi-mediated allelic trans-interaction at the imprinted Rtl1/Peg11 locus
Source:
Elsevier Ltd.
The Type 3 Deiodinase: Epigenetic Control of Brain Thyroid Hormone Action and Neurological Function.
Source:
MDPI AG
THE PLACENTA IN ABNORMALITIES AND DISORDERS OF THE FETUS
Source:
Elsevier
Placentomegaly in paternal uniparental disomy for human chromosome 14.
Source:
Elsevier BV
Novel microdeletions on chromosome 14q32.2 suggest a potential role for non-coding RNAs in Kagami-Ogata syndrome.
Source:
Springer Science and Business Media LLC
The role of genomic imprinting in biology and disease: an expanding view
Source:
Springer Science and Business Media LLC
Relative frequency of underlying genetic causes for the development of UPD(14)pat-like phenotype.
Source:
Springer Science and Business Media LLC
Kagami–Ogata syndrome: a clinically recognizable upd(14)pat and related disorder affecting the chromosome 14q32.2 imprinted region
Source:
Springer Science and Business Media LLC
Imprinted microRNA genes transcribed antisense to a reciprocally imprinted retrotransposon-like gene.
Source:
Springer Science and Business Media LLC
Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami–Ogata syndrome)
Source:
Springer Science and Business Media LLC
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