(Q34242720)

31 July 2017

1 reference

title

Endocrine aspects of the 22q11.2 deletion syndrome (English)

1 reference

31 July 2017

Weinzimer SA

1

1 reference

31 July 2017

language of work or name

English

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publication date

1 January 2001

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31 July 2017

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31 July 2017

volume

3

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31 July 2017

issue

1

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31 July 2017

page(s)

19-22

1 reference

https://scigraph.springernature.com/pub.10.1097/00125817-200101000-00005

31 July 2017

exact match

0 references

cites work

Prediction of persistent immunodeficiency in the DiGeorge anomaly

1 reference

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The DiGeorge syndrome. I. Clinical evaluation and course of partial and complete forms of the syndrome

21 January 2018

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Variable phenotypes in velocardiofacial syndrome with chromosomal deletion.

21 January 2018

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

21 January 2018

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Velo-cardio-facial syndrome: a review of 120 patients.

21 January 2018

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Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome

21 January 2018

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https://api.crossref.org/works/10.1097%2F00125817-200101000-00005

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%2F00125817-200101000-00005

The spectrum of the DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00005

Unmasking of hypoparathyroidism in familial partial DiGeorge syndrome by challenge with disodium edetate

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00005

Latent hypoparathyroidism in children with conotruncal cardiac defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00005

Idiopathic hypoparathyroidism in two patients with 22q11 microdeletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00005

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

21 January 2018

1 reference

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Brain anomalies in velo-cardio-facial syndrome

21 January 2018

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

21 January 2018

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DiGeorge syndrome: part of CATCH 22.

21 January 2018

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Thyroid abnormalities as a feature of DiGeorge syndrome: a patient report and review of the literature.

21 January 2018

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The ultimobranchial gland and congenital thyroid abnormalities in man.

21 January 2018

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Cardiovascular malformations in DiGeorge syndrome (congenital absence of hypoplasia of the thymus)

21 January 2018

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Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication?

21 January 2018

1 reference

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Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: a new component manifestation of deletion 22q11?

21 January 2018

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Hypocalcemia in critically ill children

21 January 2018

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Transient congenital hypoparathyroidism: resolution and recurrence in chromosome 22q11 deletion

21 January 2018

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Hypoparathyroidism as the major manifestation in two patients with 22q11 deletions

21 January 2018

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Velocardiofacial syndrome presenting as hypocalcemia in early adolescence

21 January 2018

1 reference

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Unmasking of latent hypoparathyroidism in a child with partial DiGeorge syndrome by ethylenediaminetetraacetic acid infusion

21 January 2018

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Cardiac malformations in the velocardiofacial syndrome

21 January 2018

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The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients

21 January 2018

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Thyrocalcitonin-containing cells in the Di George anomaly

21 January 2018

1 reference

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Congenital Cardiovascular Disease and Anomalies of the Third and Fourth Pharyngeal Pouch

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00005

Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00005

Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (digeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00005

Arthritis associated with deletion of 22q11.2: more common than previously suspected

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00005

10.1097/00125817-200101000-00005

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

31 July 2017

1003592967

0 references

1 reference