(Q33682336)

28 July 2017

title

Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion (English)

1 reference

28 July 2017

1 reference

Van Hemel JO

1

1 reference

28 July 2017

Schaap C

2

1 reference

28 July 2017

Van Opstal D

3

1 reference

28 July 2017

Mulder MP

4

1 reference

28 July 2017

Niermeijer MF

5

1 reference

28 July 2017

Meijers JH

6

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 August 1995

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

32

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28 July 2017

issue

8

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28 July 2017

page(s)

657-658

1 reference

describes a project that uses

28 July 2017

fluorescence in situ hybridization

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DiGeorge syndrome: part of CATCH 22.

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051646

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=1051646

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=1051646

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051646

A prospective cytogenetic study of 36 cases of DiGeorge syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051646

Possible role for COMT in psychosis associated with velo-cardio-facial syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051646

Antenatal diagnosis of DiGeorge syndrome

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7473663

12 December 2020

inferred from PubMed ID database lookup

Deletions within chromosome 22q11 in familial congenital heart disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7473663

12 December 2020

inferred from PubMed ID database lookup

Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7473663

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/JMG.32.8.657

1 reference

28 July 2017

1 reference

28 July 2017

1 reference