(Q83163623)

English

Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays

scientific article published on 01 May 2006

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author name string

Jeffrey E Ming

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Elizabeth Geiger

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Alison C James

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Karen L Ciprero

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Manjunath Nimmakayalu

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Yi Zhang

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Andrew Huang

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Madhavi Vaddi

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Eric Rappaport

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Elaine H Zackai

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Tamim H Shaikh

11

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

1 May 2006

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

27

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

467-473

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

The genetics of mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

21 January 2018

Whole genome DNA copy number changes identified by high density oligonucleotide arrays

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

21 January 2018

Genomic microarrays in human genetic disease and cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosome aberrations in solid tumors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Subtelomeric rearrangements detected in patients with idiopathic mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

A 2.3 Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected by standard karyotype.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Myoclonus in a patient with a deletion of the epsilon-sarcoglycan locus on chromosome 7q21

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Diagnostic genome profiling in mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosomal anomalies on 6p25 in iris hypoplasia and Axenfeld-Rieger syndrome patients defined on a purpose-built genomic microarray

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Structure of chromosomal duplicons and their role in mediating human genomic disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpoints

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular karyotyping using an SNP array for genomewide genotyping.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

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%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Segmental duplications and copy-number variation in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Assembly of microarrays for genome-wide measurement of DNA copy number

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Whole genome SNP arrays using DNA derived from formalin-fixed, paraffin-embedded ovarian tumor tissue

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20322

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.20322

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16619270%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:16619270%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q83163623&oldid=1753514188"