(Q83189066)

English

A novel competitive fluorescent multiplex STR polymorphism assay for rapid, reliable and single-tube screening of 22q11.2 copy-number aberrations

scientific article published on 01 February 2009

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19145597%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

A novel competitive fluorescent multiplex STR polymorphism assay for rapid, reliable and single-tube screening of 22q11.2 copy-number aberrations (English)

1 reference

Europe PubMed Central

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19 January 2020

author name string

Chi Yang

1

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19 January 2020

Li Shen

2

1 reference

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19 January 2020

Zhengfeng Xu

3

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19 January 2020

Xiaojian Wu

4

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19 January 2020

Xuming Mo

5

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19 January 2020

Jingjing Zhang

6

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19 January 2020

Dongjin Wang

7

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19 January 2020

Yaping Wang

8

1 reference

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19 January 2020

Yuzhu Peng

9

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19 January 2020

Li Cao

10

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19 January 2020

Yongzhong Jiang

11

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19 January 2020

Haitao Gu

12

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19 January 2020

Shilin Chen

13

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19 January 2020

Xuming Bian

14

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19 January 2020

Juntao Liu

15

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19 January 2020

Di Qiao

16

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19 January 2020

Long Yi

17

1 reference

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19 January 2020

publication date

1 February 2009

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19 January 2020

Electrophoresis

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19 January 2020

30

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19 January 2020

3

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19 January 2020

465-471

1 reference

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19 January 2020

Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Microduplication and triplication of 22q11.2: a highly variable syndrome

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletion of chromosome 22q11.2 and outcome in patients with pulmonary atresia and ventricular septal defect

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial deletions of chromosome 22q11

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pedia

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel, single nucleotide polymorphism-based assay to detect 22q11 deletions.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: a comparison

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

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/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Screening for subtelomeric rearrangements using automated fluorescent genotyping of microsatellite markers: a Lebanese study.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of two novel large deletions in SLC3A1 by semi-quantitative fluorescent multiplex PCR

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

The determination of the sequences present in the shadow bands of a dinucleotide repeat PCR.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

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/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Tandem repeats finder: a program to analyze DNA sequences

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Guideline to reference gene selection for quantitative real-time PCR

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

A common molecular basis for rearrangement disorders on chromosome 22q11

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

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/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA)

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomalies

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200800321

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/ELPS.200800321

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19145597%20AND%20SRC:MED&resulttype=core&format=json

19 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:19145597%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

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