(Q70765937)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8513333%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

title

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8513333%20AND%20SRC:MED&resulttype=core&format=json

Beckwith-Wiedemann syndrome

13 October 2019

main subject

1 reference

human embryonic development

inferred from title

1 reference

Ohlsson R

1

1 reference

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13 October 2019

Nyström A

2

1 reference

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13 October 2019

Pfeifer-Ohlsson S

3

1 reference

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13 October 2019

Töhönen V

4

1 reference

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13 October 2019

Hedborg F

5

1 reference

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13 October 2019

Schofield P

6

1 reference

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13 October 2019

Flam F

7

1 reference

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13 October 2019

Ekström TJ

8

1 reference

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13 October 2019

publication date

1 May 1993

1 reference

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13 October 2019

1 reference

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13 October 2019

volume

4

1 reference

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13 October 2019

issue

1

1 reference

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13 October 2019

page(s)

94-97

1 reference

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Genomic imprinting: developmental significance and molecular mechanism

13 October 2019

cites work

1 reference

7 January 2021

Differential imprinting and expression of maternal and paternal genomes

1 reference

7 January 2021

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

1 reference

7 January 2021

Parental imprinting of the mouse H19 gene

1 reference

7 January 2021

Parental imprinting of the mouse insulin-like growth factor II gene.

1 reference

7 January 2021

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

1 reference

7 January 2021

Monoallelic expression of the human H19 gene

1 reference

7 January 2021

Parental imprinting of the human H19 gene

1 reference

7 January 2021

Genomic imprinting and genetic disorders in man.

1 reference

7 January 2021

Beckwith-Wiedemann syndrome, tumourigenesis and imprinting

1 reference

7 January 2021

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

1 reference

7 January 2021

Dads and disomy and disease

1 reference

7 January 2021

Insulin-like growth factor 2 and short-range stimulatory loops in control of human placental growth

1 reference

7 January 2021

Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility

1 reference

7 January 2021

Genomic imprinting and the strange case of the insulin-like growth factor II receptor

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0593-94

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8513333%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference