Diagnostic evaluation of developmental delay/mental retardation: An overview (Q35057630)

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Language	Label	Description	Also known as
English	Diagnostic evaluation of developmental delay/mental retardation: An overview	scientific article

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instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12561053

retrieved

6 August 2017

review article

1 reference

stated in

Europe PubMed Central

title

Diagnostic evaluation of developmental delay/mental retardation: An overview (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12561053

retrieved

6 August 2017

author name string

Agatino Battaglia

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12561053

retrieved

6 August 2017

John C Carey

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12561053

retrieved

6 August 2017

publication date

1 February 2003

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12561053

retrieved

6 August 2017

published in

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12561053

retrieved

6 August 2017

volume

117C

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12561053

retrieved

6 August 2017

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12561053

retrieved

6 August 2017

page(s)

3-14

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12561053

retrieved

6 August 2017

cites work

The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.C.10015

retrieved

21 January 2018

Maternal uniparental disomy for chromosome 14 in a boy with a normal karyotype

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.C.10015

retrieved

21 January 2018

Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.C.10015

retrieved

21 January 2018

Identifiers

DOI

10.1002/AJMG.C.10015

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12561053

retrieved

6 August 2017

PubMed publication ID

12561053

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12561053

retrieved

6 August 2017

ResearchGate publication ID

10922953

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