(Q52917782)

9 May 2018

title

Expanding the phenotype of feingold syndrome-2. (English)

1 reference

9 May 2018

author name string

Lauren E Grote

series ordinal

1

1 reference

9 May 2018

Elena A Repnikova

series ordinal

2

1 reference

9 May 2018

Shivarajan M Amudhavalli

series ordinal

3

1 reference

9 May 2018

language of work or name

English

0 references

publication date

11 September 2015

1 reference

9 May 2018

American Journal of Medical Genetics

published in

1 reference

9 May 2018

volume

167A

1 reference

9 May 2018

issue

12

1 reference

9 May 2018

page(s)

3219-3225

1 reference

9 May 2018

Feingold syndrome associated with two novel MYCN mutations in sporadic and familial cases including monozygotic twins.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37368

Feingold syndrome: clinical review and genetic mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37368

Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37368

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37368

A fourth case of Feingold syndrome type 2: psychiatric presentation and management.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37368

Tetralogy of Fallot, microcephaly, short stature and brachymesophalangy is associated with hemizygous loss of noncoding MIR17HG and coding GPC5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37368

Genotype-phenotype correlations in MYCN-related Feingold syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37368

Twelve new patients with 13q deletion syndrome: genotype-phenotype analyses in progress.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37368

Expression of the cell surface proteoglycan glypican-5 is developmentally regulated in kidney, limb, and brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37368

Clinical features associated with a 15.41 Mb deletion of chromosome 13q encompassing the MIR17HG locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37368

A novel microdeletion involving the 13q31.3-q32.1 region in a patient with normal intelligence

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37368

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.37368

1 reference

9 May 2018

release_aau67xtaj5d7lkvlfqpvc6rpgu

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/aau67xtaj5d7lkvlfqpvc6rpgu

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

9 May 2018