(Q83367556)

English

Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery

scientific article published on 19 February 2009

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

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Yali Hu

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Xiangyu Zhu

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Yuehua Yang

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Xuming Mo

4

1 reference

Europe PubMed Central

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21 January 2020

Min Sheng

5

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Jincui Yao

6

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Dongjing Wang

7

1 reference

Europe PubMed Central

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21 January 2020

publication date

19 February 2009

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Cardiology in the Young

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

19

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21 January 2020

2

1 reference

Europe PubMed Central

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21 January 2020

179-184

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109003667

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109003667

7 January 2021

based on heuristic

inferred from DOI database lookup

MLPA analysis for the detection of deletions, duplications and complex rearrangements in the dystrophin gene: potential and pitfalls.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109003667

7 January 2021

based on heuristic

inferred from DOI database lookup

Quantitative real-time PCR technique for rapid prenatal diagnosis of Down syndrome

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109003667

7 January 2021

based on heuristic

inferred from DOI database lookup

New tetranucleotide STRP markers for detecting the 22q11.2 deletion.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109003667

7 January 2021

based on heuristic

inferred from DOI database lookup

Detailed analysis of 22q11.2 with a high density MLPA probe set

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109003667

7 January 2021

based on heuristic

inferred from DOI database lookup

The 22q11 deletion syndromes

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109003667

7 January 2021

based on heuristic

inferred from DOI database lookup

The genetics of congenital heart disease: a review of recent developments.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109003667

7 January 2021

based on heuristic

inferred from DOI database lookup

Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109003667

7 January 2021

based on heuristic

inferred from DOI database lookup

The fate of children with microdeletion 22q11.2 syndrome and congenital heart defect: clinical course and cardiac outcome

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109003667

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletion 22q11: spectrum of associated disorders

1 reference

https://api.crossref.org/works/10.1017%2FS1047951109003667

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1017/S1047951109003667

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19224675%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

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