(Q33675087)

28 July 2017

"CATCH 22" sans cardiac anomaly, thymic hypoplasia, cleft palate, and hypocalcaemia: cAtch 22. A common result of 22q11 deficiency? (English)

1 reference

28 July 2017

1 reference

Lipson A

1

1 reference

28 July 2017

Emanuel B

2

1 reference

28 July 2017

Colley P

3

1 reference

28 July 2017

Fagan K

4

1 reference

28 July 2017

Driscoll DA

5

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 September 1994

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

31

1 reference

28 July 2017

741

1 reference

28 July 2017

9

1 reference

DiGeorge syndrome: part of CATCH 22.

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050092

Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050092

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050092

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050092

DiGeorge syndrome: an historical review of clinical and cytogenetic features

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050092

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050092

Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050092

Variable phenotypes in velocardiofacial syndrome with chromosomal deletion.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050092

Maldescent of the thymus: 34 necropsy and 10 surgical cases, including 7 thymuses medial to the mandible

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7815448

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.31.9.741

1 reference

28 July 2017

1 reference

28 July 2017

1 reference