(Q41769809)

9 October 2017

Towards earlier diagnosis of 22q11 deletions (English)

1 reference

9 October 2017

Tobias ES

1

1 reference

9 October 2017

Morrison N

series ordinal

2

1 reference

9 October 2017

Whiteford ML

series ordinal

3

1 reference

9 October 2017

Tolmie JL

series ordinal

4

1 reference

9 October 2017

language of work or name

English

0 references

publication date

1 December 1999

1 reference

Archives of Disease in Childhood

9 October 2017

1 reference

9 October 2017

81

1 reference

9 October 2017

6

1 reference

9 October 2017

513-514

1 reference

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

9 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1718153

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1718153

Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2: report of five families with a review of the literature

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1718153

Chromosome 22q11 microdeletions in tetralogy of Fallot

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1718153

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1718153

6 June 2018

Identifiers

DOI

10.1136/ADC.81.6.513

1 reference

9 October 2017

1 reference

9 October 2017

PubMed publication ID

10569971

1 reference