(Q51953583)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12210300%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patient (English)

1 reference

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12 November 2019

1

1 reference

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12 November 2019

7

Marc Jeanpierre

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12210300%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

author name string

Laurence Cuisset

2

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12 November 2019

Maryse Cartigny

3

1 reference

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12 November 2019

Dominique Le Tessier

4

1 reference

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12 November 2019

Christian Vasseur

5

1 reference

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12 November 2019

Didier Rabineau

6

1 reference

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12 November 2019

publication date

1 September 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12210300%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part A

12 November 2019

published in

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12 November 2019

volume

111

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12 November 2019

issue

4

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12 November 2019

page(s)

405-408

1 reference

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Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes

12 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10570

Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10570

Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10570

Genomic imprinting related to prenatal diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10570

Human PEG1/MEST, an imprinted gene on chromosome 7

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10570

Second observation of Silver-Russel syndrome in a carrier of a reciprocal translocation with one breakpoint at site 17q25

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10570

Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10570

Severe Silver-Russell syndrome and translocation (17;20) (q25;q13)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10570

Genetics of Silver-Russell Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10570

Biallelic expression of IGFBP1 and IGFBP3, two candidate genes for the Silver-Russell syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10570

Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10570

21 January 2018

Identifiers

DOI

10.1002/AJMG.10570

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12210300%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference