(Q42668051)

4 November 2017

Monozygotic twins with chromosome 22q11 deletion and discordant phenotype (English)

1 reference

4 November 2017

4

1 reference

4 November 2017

1

Goodship J

1 reference

4 November 2017

Cross I

2

1 reference

PMCID

1051680

4 November 2017

Scambler P

series ordinal

3

1 reference

PMCID

1051680

4 November 2017

language of work or name

English

0 references

publication date

1 September 1995

1 reference

Journal of Medical Genetics

4 November 2017

1 reference

4 November 2017

32

1 reference

4 November 2017

9

1 reference

4 November 2017

746-748

1 reference

Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.

4 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051680

DiGeorge syndrome: part of CATCH 22.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051680

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051680

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051680

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051680

Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051680

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051680

Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051680

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051680

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051680

Congenital heart defects and twinning

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051680

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

3 November 2018

1 reference

12 December 2020

Characterization of a panel of highly variable minisatellites cloned from human DNA

1 reference

12 December 2020

Deletions within chromosome 22q11 in familial congenital heart disease

1 reference

12 December 2020

Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.32.9.746

1 reference

4 November 2017

1 reference

4 November 2017

1 reference

PMCID

1051680