The general anesthesia experience of deletion 8p syndrome patient -A case report-. (Q39214524)

10 September 2017

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The general anesthesia experience of deletion 8p syndrome patient -A case report-. (English)

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10 September 2017

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Woo Jong Shin

1

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10 September 2017

Sang Duk Kim

series ordinal

2

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10 September 2017

Kyoung Hun Kim

series ordinal

3

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10 September 2017

language of work or name

English

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publication date

22 October 2011

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Korean Journal of Anesthesiology

10 September 2017

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10 September 2017

61

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10 September 2017

4

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10 September 2017

332-335

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Creative Commons Attribution-NonCommercial 3.0 Unported

10 September 2017

start time

1 January 2011

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3219781

8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3219781

Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndrome.

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3219781

Difficult tracheal intubation in obstetrics

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3219781

Distal 8p deletion (8p23.1----8pter): a common deletion?

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3219781

Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3219781

Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13).

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3219781

A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3219781

Two patients with atypical interstitial deletions of 8p23.1: mapping of phenotypical traits

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3219781

Anesthetic management with laryngeal mask in a child with Brachmann-de Lange syndrome

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3219781

Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature

21 August 2018

1 reference

12 December 2020

Anaesthetic implications of Cornelia de Lange syndrome

1 reference

12 December 2020

1 reference

12 December 2020

[A patient with Cornelia de Lange syndrome with difficulty in orotracheal intubation]

1 reference

12 December 2020

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects

1 reference

12 December 2020

10.4097/KJAE.2011.61.4.332

Identifiers

DOI

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10 September 2017

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10 September 2017

PubMed publication ID

22110888

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