(Q38728522)

5 September 2017

title

Whole Exome Sequencing in Pediatric Neurology Patients: Clinical Implications and Estimated Cost Analysis (English)

1 reference

5 September 2017

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26863999%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

author name string

Martha Carlson

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26863999%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

publication date

10 February 2016

1 reference

Journal of Child Neurology

5 September 2017

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26863999%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

volume

31

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26863999%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26863999%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

page(s)

887-894

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26863999%20AND%20SRC:MED&resulttype=core&format=json

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

12 June 2020

cites work

1 reference

https://api.crossref.org/works/10.1177%2F0883073815627880

Next-generation sequencing: methodology and application

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073815627880

Clinical whole exome sequencing in child neurology practice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073815627880

The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073815627880

The promise of whole-exome sequencing in medical genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073815627880

The metabolic evaluation of the child with an intellectual developmental disorder: diagnostic algorithm for identification of treatable causes and new digital resource

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073815627880

Inborn errors of metabolism in infancy: a guide to diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073815627880

Personalized medicine approaches in epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073815627880

21 January 2018

Identifiers

DOI

10.1177/0883073815627880

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26863999%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

1 reference