(Q51940679)

English

Fine mapping and clinical reevaluation of a Brazilian pedigree with a severe form of X-linked mental retardation associated with other neurological dysfunction.

scientific article published in June 2004

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

Fine mapping and clinical reevaluation of a Brazilian pedigree with a severe form of X-linked mental retardation associated with other neurological dysfunction. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

4

object named as

Mayana Zatz

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

Maria Rita Passos-Bueno

6

object named as

Maria Rita Passos-Bueno

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

author name string

Todd S Zorick

1

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

Suzana Kleimann

2

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

A Sertié

3

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

Sérgio Rosenberg

5

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

language of work or name

0 references

publication date

1 June 2004

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

American Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

127A

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

3

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

321-323

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30009

21 January 2018

Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30009

21 January 2018

Monogenic causes of X-linked mental retardation.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30009

21 January 2018

Novel syndromic form of X-linked complicated spastic paraplegia

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30009

21 January 2018

Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30009

21 January 2018

In search of the MRX genes

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30009

21 January 2018

Identifiers

10.1002/AJMG.A.30009

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/15150789

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q51940679&oldid=2186980579"