(Q52085444)

English

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

scientific article published on 23 November 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

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

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

1 reference

based on heuristic

inferred from title

4

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

author name string

Sólveig Oskarsdóttir

1

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

Christina Persson

2

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

Bengt O Eriksson

3

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

publication date

23 November 2004

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

164

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

3

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

146-153

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

https://scigraph.springernature.com/pub.10.1007/s00431-004-1577-8

0 references

Skeletal anomalies and deformities in patients with deletions of 22q11

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 22q11.2 deletion syndrome

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymicrogyria in chromosome 22q11 deletion syndrome.

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pediatric testicular problems

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved technique for chromosome preparations from human lymphocytes

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pediatric hernias and hydroceles

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genitourinary malformations in chromosome 22q11.2 deletion

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The annual incidence of DiGeorge/velocardiofacial syndrome

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoparathyroidism and 22q11 deletion syndrome

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-004-1577-8

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

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

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