(Q46819083)

25 December 2017

title

Age-dependent clinical problems in a Norwegian national survey of patients with the 22q11.2 deletion syndrome (English)

1 reference

25 December 2017

2

Ivar Følling

1 reference

25 December 2017

5

Tore G Abrahamsen

1 reference

25 December 2017

author name string

Kari Lima

series ordinal

1

1 reference

25 December 2017

Kristin L Eiklid

series ordinal

3

1 reference

25 December 2017

Solveig Natvig

series ordinal

4

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25 December 2017

publication date

26 February 2010

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25 December 2017

European Journal of Pediatrics

published in

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25 December 2017

volume

169

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25 December 2017

issue

8

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25 December 2017

page(s)

983-989

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25 December 2017

Prevalence of duplications and deletions of the 22q11 DiGeorge syndrome region in a population-based sample of infants with cleft palate

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00431-010-1161-3

Distal 22q11.2 microduplication encompassing the BCR gene.

21 January 2018

1 reference

12 December 2020

Birthweight by gestational age in Norway

1 reference

12 December 2020

Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome

1 reference

12 December 2020

Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

1 reference

12 December 2020

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

1 reference

12 December 2020

Decreased thymus size in formula-fed infants compared with breastfed infants

1 reference

12 December 2020

Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes

1 reference

12 December 2020

Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.

1 reference

12 December 2020

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence

1 reference

12 December 2020

Role of TBX1 in human del22q11.2 syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Scoliosis in velo-cardio-facial syndrome.

1 reference

12 December 2020

Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update

1 reference

12 December 2020

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

1 reference

12 December 2020

Communication issues in 22q11.2 deletion syndrome: children at risk.

1 reference

12 December 2020

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

1 reference

12 December 2020

Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution

1 reference

12 December 2020

A population study of chromosome 22q11 deletions in infancy

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies

1 reference

12 December 2020

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

1 reference

12 December 2020

Attention deficits in children with 22q.11 deletion syndrome.

1 reference

12 December 2020

Melatonin therapy for circadian rhythm sleep disorders in children with multiple disabilities: what have we learned in the last decade?

1 reference

12 December 2020

Defining the clinical spectrum of deletion 22q11.2

1 reference

12 December 2020

Breast-feeding influences thymic size in late infancy

1 reference

12 December 2020

Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED.

1 reference

12 December 2020

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

1 reference

12 December 2020

Detailed analysis of 22q11.2 with a high density MLPA probe set

1 reference

12 December 2020

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion

1 reference

12 December 2020

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

1 reference

12 December 2020

Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group

1 reference

12 December 2020

The annual incidence of DiGeorge/velocardiofacial syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00431-010-1161-3

Identifiers

DOI

1 reference

25 December 2017

1 reference

25 December 2017