(Q40016309)

16 September 2017

title

Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/H19 in Silver-Russell syndrome (English)

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16 September 2017

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K Kannenberg

1

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16 September 2017

C Urban

series ordinal

2

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16 September 2017

G Binder

series ordinal

3

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16 September 2017

publication date

8 February 2012

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16 September 2017

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16 September 2017

volume

81

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16 September 2017

issue

4

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16 September 2017

page(s)

366-377

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Role for DNA methylation in genomic imprinting

16 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01844.X

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Effect of long-term growth hormone treatment on final height of children with Russell-Silver syndrome.

21 January 2018

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Epigenetic decisions in mammalian germ cells.

21 January 2018

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Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.

21 January 2018

1 reference

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21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01844.X

Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01844.X

Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci

21 January 2018

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Methylation profiling in individuals with Russell-Silver syndrome.

21 January 2018

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21 January 2018

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Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

21 January 2018

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MLPA and MAPH: new techniques for detection of gene deletions

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A census of mammalian imprinting.

21 January 2018

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Analysis of allelic differential expression in human white blood cells

21 January 2018

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LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

21 January 2018

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Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9

21 January 2018

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The C15orf2 gene in the Prader-Willi syndrome region is subject to genomic imprinting and positive selection

21 January 2018

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Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

21 January 2018

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Zac1 regulates an imprinted gene network critically involved in the control of embryonic growth

21 January 2018

1 reference

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Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome.

21 January 2018

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A comprehensive microarray-based DNA methylation study of 367 hematological neoplasms

21 January 2018

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21 January 2018

Identifiers

DOI

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16 September 2017

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