Searching for genomic variants in IGF2 and CDKN1C in Silver-Russell syndrome patients (Q47247208)

12 January 2018

title

Searching for genomic variants in IGF2 and CDKN1C in Silver-Russell syndrome patients (English)

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main subject

Silver-Russell syndrome

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Caitriona Obermann

1

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12 January 2018

Esther Meyer

2

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Sebastian Prager

3

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Jürgen Tomiuk

4

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Hartmut A Wollmann

5

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12 January 2018

Thomas Eggermann

6

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publication date

1 July 2004

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Molecular Genetics and Metabolism

published in

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12 January 2018

volume

82

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page(s)

246-250

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issue

3

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12 January 2018

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

cites work

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.008

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

7 January 2021

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Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.008

Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.008

Placental-specific IGF-II is a major modulator of placental and fetal growth.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.008

Growth and symptoms in Silver-Russell syndrome: review on the basis of 386 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.008

Screening for mutations in the promoter and the coding region of the IGFBP1 and IGFBP3 genes in Silver-Russell syndrome patients.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.008

Positive associations between single nucleotide polymorphisms in the IGF2 gene region and body mass index in adult males

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.008

GENEPOP (Version 1.2): Population Genetics Software for Exact Tests and Ecumenicism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.008

Analysis of CDKN1C in Beckwith Wiedemann syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.04.008

10.1016/J.YMGME.2004.04.008

7 January 2021

Identifiers

DOI

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12 January 2018

PubMed ID

15234339

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12 January 2018