(Q33679201)

28 July 2017

1 reference

title

A report of a child with a deletion (9)(q34.3): a recognisable phenotype? (English)

1 reference

28 July 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9222977

chromosomal deletion syndrome

7 November 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9222977

7 November 2024

author name string

H. Ayyash

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9222977

7 November 2024

R. Mueller

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9222977

7 November 2024

E. Maltby

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9222977

7 November 2024

P. Horsfield

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9222977

7 November 2024

N. Telford

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9222977

7 November 2024

R. Tyler

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9222977

7 November 2024

language of work or name

English

0 references

publication date

1 July 1997

1 reference

28 July 2017

July 1997

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9222977

full work available at URL

7 November 2024

https://jmg.bmj.com/content/jmedgenet/34/7/610.full.pdf

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9222977

https://europepmc.org/articles/PMC1051009

7 November 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9222977

https://europepmc.org/articles/PMC1051009?pdf=render

7 November 2024

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9222977

https://syndication.highwire.org/content/doi/10.1136/jmg.34.7.610

7 November 2024

1 reference

https://api.crossref.org/works/10.1136/JMG.34.7.610

Journal of Medical Genetics

7 November 2024

published in

1 reference

28 July 2017

volume

34

1 reference

28 July 2017

issue

7

1 reference

28 July 2017

page(s)

610-612

1 reference

Infant with multiple congenital anomalies and deletion (9)(q34.3).

28 July 2017

cites work

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051009

Patients with deletions of 9q22q34 do not define a syndrome: three case reports and a literature review

21 June 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051009

Intercalary deletions of 9q

21 June 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051009

21 June 2018

Identifiers

DOI

10.1136/JMG.34.7.610

1 reference

28 July 2017

1 reference

28 July 2017

1 reference