(Q24675242)

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Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

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title

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden (English)

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main subject

obstetrics and gynaecology

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Sweden

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22q11 deletion syndrome

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S Oskarsdóttir

1

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M Vujic

series ordinal

2

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A Fasth

series ordinal

3

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language of work or name

English

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publication date

February 2004

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published in

Archives of Disease in Childhood

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volume

89

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issue

2

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page(s)

148-51

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cites work

The Philadelphia story: the 22q11.2 deletion: report on 250 patients

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1719787

retrieved

7 April 2017

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1719787

retrieved

7 April 2017

The 22q11 deletion syndromes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1719787

retrieved

28 September 2017

A population study of chromosome 22q11 deletions in infancy

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1719787

retrieved

28 September 2017

Prevalence of 22q11 microdeletion

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1719787

retrieved

28 September 2017

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1719787

retrieved

28 September 2017

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1719787

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28 September 2017

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1719787

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28 September 2017

Towards earlier diagnosis of 22q11 deletions

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1719787

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30 May 2018

The annual incidence of DiGeorge/velocardiofacial syndrome

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1719787

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30 May 2018

An improved technique for chromosome preparations from human lymphocytes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14736631

retrieved

12 December 2020

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(Q24675242)

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

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