(Q73356663)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

R C Marinescu

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

E I Johnson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

D Grady

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

X N Chen

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

J Overhauser

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

publication date

1 October 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

volume

56

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

page(s)

282-288

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

Cytologic observations in 35 individuals with a 5p- karyotype

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

A yeast artificial chromosome contig of the critical region for cri-du-chat syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

A high-resolution physical and transcript map of the Cri du chat region of human chromosome 5p.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

Multicolor Spectral Karyotyping of Human Chromosomes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

Molecular and phenotypic mapping of the short arm of chromosome 5: sublocalization of the critical region for the cri-du-chat syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

Identification of cryptic rearrangements in patients with 18q- deletion syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560405.X

7 January 2021

10.1034/J.1399-0004.1999.560405.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10636446%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference