(Q36938711)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17850622%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

review article

1 reference

title

The impact of array genomic hybridization on mental retardation research: a review of current technologies and their clinical utility (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17850622%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17850622%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Jan M Friedman

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17850622%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

author name string

Zahir F

series ordinal

1

1 reference

17 August 2017

Friedman JM

series ordinal

2

1 reference

17 August 2017

publication date

1 October 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17850622%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17850622%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

volume

72

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17850622%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17850622%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

page(s)

271-287

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17850622%20AND%20SRC:MED&resulttype=core&format=json

BAC array CGH reveals genomic aberrations in idiopathic mental retardation.

7 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2007.00847.X

Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2007.00847.X

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2007.00847.X

Practice parameter: evaluation of the child with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and The Practice Committee of the Child Neurology Society.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2007.00847.X

Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2007.00847.X

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2007.00847.X

Common deletion polymorphisms in the human genome.

21 January 2018

1 reference

COCI

https://opencitations.net/index/coci/api/v1/citations/10.1038/NG1696

Global variation in copy number in the human genome

30 October 2021

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/NATURE05329

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

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/NG754

Initial sequencing and analysis of the human genome

1 reference

28 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/35057062

Identifiers

DOI

10.1111/J.1399-0004.2007.00847.X

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17850622%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference