(Q51975040)

English

Dystonia in a patient with deletion of 18p.

scientific article published in April 1998

In more languages

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

Dystonia in a patient with deletion of 18p. (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

author name string

Tezzon F

1

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

Zanoni T

2

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

Passarin MG

3

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

Ferrari G

4

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

publication date

1 April 1998

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

Italian journal of neurological sciences

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

19

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

2

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

90-93

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34

1 reference

https://pubmed.ncbi.nlm.nih.gov/10935843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 18 p-syndrome. Report of four cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/10935843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution

1 reference

https://pubmed.ncbi.nlm.nih.gov/10935843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pituitary dwarfism and "Goldenhar type= multiple deformities in a patient with deletion of the short arm of chromosome 18

1 reference

https://pubmed.ncbi.nlm.nih.gov/10935843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 18p- syndrome. Report of five cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/10935843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[18p-syndrome with bilateral pyramidal tract signs, dystonia of the lower extremities and concentric visual field defect]

1 reference

https://pubmed.ncbi.nlm.nih.gov/10935843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/10935843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epileptic seizures, arthrogryposis, and migrational brain disorders: a syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/10935843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sporadic focal dystonia in northwest Germany: molecular basis on chromosome 18p

1 reference

https://pubmed.ncbi.nlm.nih.gov/10935843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02427563

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/10935843

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