Narrowing the candidate region for congenital diaphragmatic hernia in chromosome 15q26: contradictory results. (Q42607970)

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8 January 2020

title

Narrowing the candidate region for congenital diaphragmatic hernia in chromosome 15q26: contradictory results (English)

1 reference

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congenital diaphragmatic hernia

8 January 2020

main subject

1 reference

2

1 reference

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8 January 2020

Corrado Romano

3

1 reference

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8 January 2020

Lucia Castiglia

1

1 reference

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8 January 2020

Ornella Galesi

4

1 reference

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8 January 2020

author name string

Grillo L

5

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8 January 2020

Sturnio M

6

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8 January 2020

Failla P

7

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8 January 2020

language of work or name

English

0 references

publication date

1 November 2005

1 reference

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American Journal of Human Genetics

8 January 2020

published in

1 reference

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volume

77

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8 January 2020

issue

5

1 reference

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8 January 2020

page(s)

892-4; author reply 894-5

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Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization

8 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1271395

Human STX polysialyltransferase forms the embryonic form of the neural cell adhesion molecule. Tissue-specific expression, neurite outgrowth, and chromosomal localization in comparison with another polysialyltransferase, PST

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1271395

Long-term outlook for survivors of congenital diaphragmatic hernia

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1271395

Distinct 15q genotypes in Russell-Silver and ring 15 syndromes

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1271395

Molecular cytogenetic characterization of ring chromosome 15 in three unrelated patients.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1271395

Congenital diaphragmatic hernia: is 15q26.1-26.2 a candidate locus?

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1271395

De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1271395

Developmental regulation of polysialic acid synthesis in mouse directed by two polysialyltransferases, PST and STX.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1271395

A prospective study of the outcome for fetuses with diaphragmatic hernia

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1271395

Polysialylated NCAM expression during motor axon outgrowth and myogenesis in the fetal rat

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16252246

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/497082

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16252246%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference

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8 January 2020

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