(Q37921180)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21861138%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

review article

1 reference

title

Head and neck manifestations of 22q11.2 deletion syndromes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21861138%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21861138%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

Udi Cinamon

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21861138%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

author name string

Yehudah Roth

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21861138%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

Abraham Goldfarb

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21861138%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

publication date

23 August 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21861138%20AND%20SRC:MED&resulttype=core&format=json

European Archives of Oto-Rhino-Laryngology

11 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21861138%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

volume

269

1 reference

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11 February 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21861138%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

page(s)

381-387

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21861138%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00405-011-1745-1

11 February 2020

exact match

0 references

cites work

Defining the clinical spectrum of deletion 22q11.2

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

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

21 January 2018

1 reference

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Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

DiGeorge syndrome: part of CATCH 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Endocrine aspects of the 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Thyroid function and morphology in subjects with microdeletion of chromosome 22q11 (del(22)(q11)).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Dissecting contiguous gene defects: TBX1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

The spectrum of the DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Clinical features of 78 adults with 22q11 Deletion Syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Thyroid gland and carotid artery anomalies in 22q11.2 deletion syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Endocrine manifestations of chromosome 22q11.2 microdeletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Parathyroid gland dysfunction in 22q11.2 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Cervical vascular and upper airway asymmetry in Velo-cardio-facial syndrome: correlation of nasopharyngoscopy with MRA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

21 January 2018

Thymus transplantation

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Upper airway asymmetry in velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Otolaryngologic manifestations of the 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Prevalence of 22q11 microdeletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Short trachea, with reduced number of cartilage rings--a hitherto unrecognized feature of DiGeorge syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Structural airway anomalies in patients with DiGeorge syndrome: a current review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

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/10.1007%2FS00405-011-1745-1

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/10.1007%2FS00405-011-1745-1

The velo-cardio-facial syndrome: the otorhinolaryngeal manifestations and implications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

B cell non-Hodgkin's lymphoma in a girl with the DiGeorge anomaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00405-011-1745-1

Dysphagia in children with a 22q11.2 deletion: unusual pattern found on modified barium swallow

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

[Insufficiency of palatolaryngeal passage as a developmental disorder.]

1 reference

12 December 2020

Malignancy in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

1 reference

12 December 2020

[Rhadboid tumours: hSNF/INI1 deficient cancers of early childhood with aggressive behaviour].

1 reference

12 December 2020

Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: report of three patients.

1 reference

12 December 2020

A deletion in chromosome 22 can cause DiGeorge syndrome

1 reference

12 December 2020

The 22q11.2 deletion syndrome

1 reference

12 December 2020

Thickness and Histologic and Histochemical Properties of the Superior Pharyngeal Constrictor Muscle in Velocardiofacial Syndrome

1 reference

12 December 2020

Graves' disease in patients with 22q11.2 deletion

1 reference

12 December 2020

DiGeorge's or the III-IV pharyngeal pouch syndrome: pathology and a theory of pathogenesis

1 reference

12 December 2020

Subglottic web in a mother and son with 22q11.2 deletion

1 reference

12 December 2020

DiGeorge syndrome associated with multiple squamous cell carcinomas

1 reference

12 December 2020

Transient congenital hypoparathyroidism and 22q11 deletion

1 reference

12 December 2020

Indications for a tumor suppressor gene at 22q11 involved in the pathogenesis of ependymal tumors and distinct from hSNF5/INI1.

1 reference

12 December 2020

22q11.2 deletion syndrome in Singapore (2000-2003): a case for active ascertainment

1 reference

12 December 2020

Allelotyping of follicular thyroid carcinoma: frequent allelic losses in chromosome arms 7q, 11p, and 22q

1 reference

12 December 2020

Low thymic output in the 22q11.2 deletion syndrome measured by CCR9+CD45RA+ T cell counts and T cell receptor rearrangement excision circles

1 reference

12 December 2020

The velo-cardio-facial syndrome: a clinical and genetic analysis

1 reference

12 December 2020