(Q52056764)

20 April 2018

review article

1 reference

title

An interstitial deletion of chromosome 7 at band q21: a case report and review. (English)

1 reference

20 April 2018

author

Markus M Nöthen

10

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20 April 2018

Wim Wuyts

object named as

Wim Wuyts

3

0 references

Frank Speleman

9

object named as

Frank Speleman

1 reference

20 April 2018

Ludwine Messiaen

4

object named as

Ludwine Messiaen

1 reference

20 April 2018

author name string

Winnie Courtens

1

1 reference

20 April 2018

Stefan Vermeulen

2

1 reference

20 April 2018

Jan Wauters

5

1 reference

20 April 2018

Lieve Nuytinck

6

1 reference

20 April 2018

Nils Peeters

7

1 reference

20 April 2018

Katrien Storm

8

1 reference

20 April 2018

language of work or name

English

0 references

publication date

1 April 2005

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20 April 2018

American Journal of Medical Genetics

published in

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20 April 2018

volume

134A

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20 April 2018

issue

1

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20 April 2018

page(s)

12-23

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20 April 2018

Gastrointestinal complications of Russell-Silver syndrome: a pilot study

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

Split hand/split foot malformation associated with sensorineural deafness, inner and middle ear malformation, hypodontia, congenital vertical talus, and deletion of eight microsatellite markers in 7q21.1-q21.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

Maternal uniparental disomy 7--review and further delineation of the phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

No evidence of submicroscopic deletion or segmental uniparental disomy within the candidate regions 7p11.2-p13 and 7q31-qter in a series of non-uniparental disomy Silver-Russell syndrome cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

Interstitial deletion of chromosome 7 detected in three unrelated patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

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.A.30106

Gene Dosage Analysis in Silver-Russell Syndrome: Use of Quantitative Competitive PCR and Dual-Color FISH to Estimate the Frequency of Duplications in 7p11.2–p13

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30106

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.30106

1 reference

20 April 2018

1 reference

20 April 2018