(Q42586619)

3 November 2017

Germline PHOX2B mutation in hereditary neuroblastoma (English)

1 reference

3 November 2017

Yael P Mosse

1

1 reference

3 November 2017

Marci Laudenslager

2

1 reference

3 November 2017

Deepa Khazi

3

1 reference

3 November 2017

Alex J Carlisle

4

1 reference

3 November 2017

Cynthia L Winter

5

1 reference

3 November 2017

Eric Rappaport

6

1 reference

3 November 2017

John M Maris

7

1 reference

3 November 2017

language of work or name

English

0 references

publication date

1 October 2004

1 reference

American Journal of Human Genetics

3 November 2017

1 reference

3 November 2017

75

1 reference

3 November 2017

727-730

1 reference

3 November 2017

4

1 reference

PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome

3 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182065

Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182065

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182065

Treatment of neuroblastoma in patients with neurocristopathy syndromes

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182065

Phox2 genes - from patterning to connectivity

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182065

Segregation at three loci explains familial and population risk in Hirschsprung disease

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182065

Molecular biology of neuroblastoma

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182065

The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182065

Coexistent neuroblastoma and Hirschsprung's disease ?Another manifestation of the neurocristopathy?

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182065

Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182065

Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15338462

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Linkage analysis in families with recurrent neuroblastoma

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15338462

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/424530

1 reference

3 November 2017

1 reference

3 November 2017

1 reference