(Q37673851)

21 August 2017

1 reference

title

Newborn screening programs: should 22q11 deletion syndrome be added? (English)

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21 August 2017

main subject

22q11 deletion syndrome

1 reference

Abigail M Bales

1

1 reference

21 August 2017

Christina A Zaleski

series ordinal

2

1 reference

21 August 2017

Elizabeth W McPherson

series ordinal

3

1 reference

21 August 2017

language of work or name

English

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publication date

1 March 2010

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21 August 2017

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21 August 2017

volume

12

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21 August 2017

issue

3

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21 August 2017

page(s)

135-144

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Newborn screening: new developments, new dilemmas.

21 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Monozygotic twins with chromosome 22q11 deletion and discordant phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

22q11 deletion syndrome: is that what they used to call . . . ?

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

The 22q11.2 deletion in African-American patients: an underdiagnosed population?

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Deletion 22q11: spectrum of associated disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Newborn screening for congenital heart defects: a systematic review and cost-effectiveness analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Presentation of congenital heart disease in infancy: implications for routine examination

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Immunodeficiency and autoimmunity in 22q11.2 deletion syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes).

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Evolution of latent hypoparathyroidism in familial 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Growth hormone deficiency in patients with 22q11.2 deletion: expanding the phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Endocrine aspects of the 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Facial features in children with the 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

DiGeorge syndrome: new insights

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Otolaryngologic manifestations of the 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

22q11.2DS deletion syndrome: developmental milestones in infants and toddlers

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Communication disorders in the 22Q11.2 microdeletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Taking advantage of early diagnosis: preschool children with the 22q11.2 deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Schizophrenia and 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia

21 January 2018

1 reference

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Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Genetic syndromes and congenital heart defects: how is surgical management affected?

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Two-year general and neurodevelopmental outcome after neonatal complex cardiac surgery in patients with deletion 22q11.2: a comparative study

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Safety of live viral vaccines in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Live viral vaccines in patients with partial DiGeorge syndrome: clinical experience and cellular immunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Velo-cardio-facial syndrome: 30 Years of study

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Clinical variability of the 22q11.2 duplication syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Newborn screening for Duchenne muscular dystrophy: a psychosocial study

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Psychosocial risk associated with newborn screening for cystic fibrosis: parents' experience while awaiting the sweat-test appointment

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

The vulnerable child syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Why tell asymptomatic children of the risk of an adult-onset disease in the family but not test them for it?

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Is earlier better? At the beginning of schizophrenia: timing and opportunities for early intervention

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Comparing the clinical and economic effects of clinical examination, pulse oximetry, and echocardiography in newborn screening for congenital heart defects: a probabilistic cost-effectiveness model and value of information analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Bronchopulmonary disease in children with cystic fibrosis after early or delayed diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Newborn screening: toward a uniform screening panel and system

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

Parathyroid function and growth in 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181CDEB9A

10.1097/GIM.0B013E3181CDEB9A

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

21 August 2017

1028885974

0 references

1 reference