(Q37004473)

17 August 2017

0 references

The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome (English)

1 reference

17 August 2017

Nadine Schönherr

1

1 reference

17 August 2017

Esther Meyer

2

1 reference

17 August 2017

Andreas Roos

3

1 reference

17 August 2017

Angela Schmidt

4

1 reference

17 August 2017

Hartmut A Wollmann

5

1 reference

17 August 2017

Thomas Eggermann

6

1 reference

17 August 2017

language of work or name

English

0 references

publication date

8 September 2006

1 reference

Journal of Medical Genetics

17 August 2017

1 reference

17 August 2017

44

1 reference

17 August 2017

1

1 reference

17 August 2017

59-63

1 reference

Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597902

Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597902

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597902

Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597902

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597902

Analysis of CDKN1C in Beckwith Wiedemann syndrome.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597902

Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597902

Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation

4 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16963484

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.2006.044370

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

16963484

1 reference