(Q51925287)

17 April 2018

title

Clinical features of 78 adults with 22q11 Deletion Syndrome. (English)

1 reference

17 April 2018

7

Michael A Gatzoulis

1 reference

17 April 2018

Oana Caluseriu

5

object named as

Oana Caluseriu

1 reference

17 April 2018

author name string

Anne S Bassett

1

1 reference

17 April 2018

Eva W C Chow

2

1 reference

17 April 2018

Janice Husted

3

1 reference

17 April 2018

Rosanna Weksberg

4

1 reference

17 April 2018

Gary D Webb

6

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17 April 2018

language of work or name

English

0 references

publication date

1 November 2005

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17 April 2018

American Journal of Medical Genetics

published in

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17 April 2018

volume

138

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17 April 2018

issue

4

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17 April 2018

page(s)

307-313

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17 April 2018

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

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22 May 2018

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22 May 2018

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Auxological evaluation in patients with DiGeorge/velocardiofacial syndrome (deletion 22q11.2 syndrome).

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22 May 2018

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

22 May 2018

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22 May 2018

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22 May 2018

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Phenotype of adults with the 22q11 deletion syndrome: A review

22 May 2018

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

22 May 2018

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

22 May 2018

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A population study of chromosome 22q11 deletions in infancy

22 May 2018

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22 May 2018

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22 May 2018

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

22 May 2018

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22 May 2018

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Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

22 May 2018

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A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome

22 May 2018

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High rates of schizophrenia in adults with velo-cardio-facial syndrome.

22 May 2018

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Frequency and predictive value of 22q11 deletion

13 August 2018

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Parathyroid function and growth in 22q11.2 deletion syndrome

13 August 2018

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Crossref

https://api.crossref.org/works/10.1002%2FAJMG.A.30984

Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region

21 January 2018

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Users' guides to the medical literature: XXIV. How to use an article on the clinical manifestations of disease. Evidence-Based Medicine Working Group

30 November 2018

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12 December 2020

Velopharyngeal incompetence and chromosome 22q11 deletion

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12 December 2020

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!

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12 December 2020

Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults

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12 December 2020

22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypes

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12 December 2020

Genetic analyses in two extended families with deletion 22q11 syndrome: importance of extracardiac manifestations

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12 December 2020

Identifiers

DOI

10.1002/AJMG.A.30984

1 reference

17 April 2018

PMC publication ID

3127862

1 reference

17 April 2018

PubMed publication ID

16208694

1 reference

17 April 2018