(Q51927420)

English

A t(4;9)(q34;p22) translocation associated with partial epilepsy, mental retardation, and dysmorphism.

scientific article published in August 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

A t(4;9)(q34;p22) translocation associated with partial epilepsy, mental retardation, and dysmorphism. (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

2

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

4

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

author name string

Pasquale Striano

1

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

Lucia Castiglia

3

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

Sabina Pelligra

5

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

Salvatore Striano

6

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

publication date

1 August 2005

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

46

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

8

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

1322-1324

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

Chromosomal abnormalities and epilepsy: a review for clinicians and gene hunters

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.64304.X

21 January 2018

Disruption of the PDGFB gene in a 1;22 translocation patient does not cause Costello syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.64304.X

21 January 2018

A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosomes 2;7 and 5;20

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.64304.X

21 January 2018

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

28 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1073/PNAS.83.9.2934

Identifiers

10.1111/J.1528-1167.2005.64304.X

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16060948

ResearchGate publication ID

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