(Q34722380)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

title

Evidence for a distinct region causing a cat-like cry in patients with 5p deletions (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

author name string

M Gersh

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

S A Goodart

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

L M Pasztor

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

D J Harris

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

L Weiss

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

J Overhauser

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

language of work or name

English

0 references

publication date

1 June 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

25 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

volume

56

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

page(s)

1404-1410

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

25 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801088

de Lange syndrome: a clinical review of 310 individuals

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801088

Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801088

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801088

Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801088

Interstitial deletion of the short arm of chromosome 5 in a mother and three children.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801088

Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801088

Terminal deletion of the short arm of chromosome 5.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801088

A fine structure physical map of the short arm of chromosome 5

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801088

Clinical and molecular diagnosis of Miller-Dieker syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801088

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801088

Parental origin of chromosome 5 deletions in the cri-du-chat syndrome

7 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7762563

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Duplication 3q syndrome: molecular delineation of the critical region

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7762563

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762563%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

PubMed publication ID

7762563

1 reference