(Q37318122)

19 August 2017

Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report (English)

1 reference

19 August 2017

1 reference

Ryan N Traylor

1

1 reference

19 August 2017

Zheng Fan

2

1 reference

19 August 2017

Beth Hudson

3

1 reference

19 August 2017

Jill A Rosenfeld

4

1 reference

19 August 2017

Lisa G Shaffer

5

1 reference

19 August 2017

Beth S Torchia

6

1 reference

19 August 2017

Blake C Ballif

7

1 reference

19 August 2017

7 August 2009

1 reference

19 August 2017

Molecular Cytogenetics

1 reference

19 August 2017

2

1 reference

19 August 2017

17

1 reference

Eph/ephrin signaling: networks.

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731778

Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731778

Multiple roles of ephrins in morphogenesis, neuronal networking, and brain function.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731778

New insights into the phenotypes of 6q deletions

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731778

A 5-Mb microdeletion at 6q16.1-q16.3 with SIM gene deletion and obesity.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731778

Autistic features with speech delay in a girl with an approximately 1.5-Mb deletion in 6q16.1, including GPR63 and FUT9.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731778

Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731778

Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731778

Interstitial 6q deletion: clinical and array CGH characterisation of a new patient.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731778

Tumour suppressor gene expression correlates with gastric cancer prognosis

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731778

2 September 2018

Identifiers

DOI

10.1186/1755-8166-2-17

1 reference

Dimensions Publication ID

19 August 2017

0 references

1 reference

19 August 2017

PubMed publication ID

19664229

1 reference