(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

Ayyash H

1

1 reference

28 July 2017

Mueller R

2

1 reference

28 July 2017

Maltby E

3

1 reference

28 July 2017

Horsfield P

4

1 reference

28 July 2017

Telford N

5

1 reference

28 July 2017

Tyler R

6

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 July 1997

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

34

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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

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

PubMed Central

reference URL

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

21 June 2018

1 reference

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

PubMed Central

reference URL

Intercalary deletions of 9q

21 June 2018

1 reference

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

PubMed Central

reference URL

21 June 2018

Identifiers

DOI

10.1136/JMG.34.7.610

1 reference

28 July 2017

1 reference

28 July 2017

1 reference