Presenting phenotype in 100 children with the 22q11 deletion syndrome. (Q52085444)

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scientific article published on 23 November 2004

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Language	Label	Description	Also known as
English	Presenting phenotype in 100 children with the 22q11 deletion syndrome.	scientific article published on 23 November 2004

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instance of

scholarly article

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Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

title

Presenting phenotype in 100 children with the 22q11 deletion syndrome. (English)

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stated in

Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

main subject

phenotype

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based on heuristic

inferred from title

author

Anders Fasth

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4

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Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

author name string

Sólveig Oskarsdóttir

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

Christina Persson

series ordinal

2

1 reference

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Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

Bengt O Eriksson

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

publication date

23 November 2004

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Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

published in

European Journal of Pediatrics

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stated in

Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

volume

164

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

issue

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

page(s)

146-153

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Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

cites work

Skeletal anomalies and deformities in patients with deletions of 22q11

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565286

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 22q11.2 deletion syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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inferred from PubMed ID database lookup

Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndrome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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inferred from PubMed ID database lookup

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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inferred from PubMed ID database lookup

Polymicrogyria in chromosome 22q11 deletion syndrome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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A prospective cross-sectional study of speech in patients with the 22q11 deletion syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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inferred from PubMed ID database lookup

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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inferred from PubMed ID database lookup

Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomalies

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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Pediatric testicular problems

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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inferred from PubMed ID database lookup

An improved technique for chromosome preparations from human lymphocytes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pediatric hernias and hydroceles

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565286

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genitourinary malformations in chromosome 22q11.2 deletion

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565286

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The annual incidence of DiGeorge/velocardiofacial syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565286

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoparathyroidism and 22q11 deletion syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15565286

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12 December 2020

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Identifiers

DOI

10.1007/S00431-004-1577-8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

PubMed publication ID

15565286

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15565286

retrieved

21 April 2018

reference URL

http://europepmc.org/abstract/MED/15565286

 

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