(Q53133318)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

title

Speech and hearing in adults with 22q11.2 deletion syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

author name string

Vanda Friman

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

Sólveig Óskarsdóttir

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

Radi Jönsson

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

language of work or name

English

0 references

publication date

19 November 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics

18 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

volume

158A

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

page(s)

3071-3079

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

Clinical features of 78 adults with 22q11 Deletion Syndrome.

18 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

Premature death in adults with 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

Upper airway asymmetry in velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

Analysis of speech characteristics in children with velocardiofacial syndrome (VCFS) and children with phenotypic overlap without VCFS

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

The annual incidence of DiGeorge/velocardiofacial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

Audiological findings in patients with microdeletion 22q11 (di George/velocardiofacial syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

Otolaryngologic manifestations of the 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

The cleft audit protocol for speech-augmented: A validated and reliable measure for auditing cleft speech.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

The prevalence of apraxia characteristics in patients with velocardiofacial syndrome as compared with other cleft populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

The neuropsychology of 22q11 deletion syndrome. A neuropsychiatric study of 100 individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

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/10.1002%2FAJMG.A.35589

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

Velopharyngeal anatomy in 22q11.2 deletion syndrome: a three-dimensional cephalometric analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

Velo-cardio-facial syndrome: 30 Years of study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35589

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.35589

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23165987%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

1 reference