(Q52244115)

English

Fragile X syndrome: a genetic etiology for developmental Gerstmann's syndrome.

scientific article published in December 1989

In more languages

edit

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2590008

retrieved

28 April 2018

reference URL

http://europepmc.org/abstract/MED/2590008

title

Fragile X syndrome: a genetic etiology for developmental Gerstmann's syndrome. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2590008

retrieved

28 April 2018

reference URL

http://europepmc.org/abstract/MED/2590008

1 reference

Grisby J

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2590008

retrieved

28 April 2018

reference URL

http://europepmc.org/abstract/MED/2590008

Haggerman R

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2590008

retrieved

28 April 2018

reference URL

http://europepmc.org/abstract/MED/2590008

publication date

1 December 1989

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2590008

retrieved

28 April 2018

reference URL

http://europepmc.org/abstract/MED/2590008

published in

Archives of Neurology

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2590008

retrieved

28 April 2018

reference URL

http://europepmc.org/abstract/MED/2590008

volume

46

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2590008

retrieved

28 April 2018

reference URL

http://europepmc.org/abstract/MED/2590008

issue

12

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2590008

retrieved

28 April 2018

reference URL

http://europepmc.org/abstract/MED/2590008

page(s)

1269-1270

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2590008

retrieved

28 April 2018

reference URL

http://europepmc.org/abstract/MED/2590008

Identifiers

DOI

10.1001/ARCHNEUR.1989.00520480011005

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2590008

retrieved

28 April 2018

reference URL

http://europepmc.org/abstract/MED/2590008

PubMed publication ID

2590008

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2590008

retrieved

28 April 2018

reference URL

http://europepmc.org/abstract/MED/2590008

(Q52244115)

Fragile X syndrome: a genetic etiology for developmental Gerstmann's syndrome.

Statements

Identifiers

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)