(Q51559597)

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The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairment.

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scholarly article

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Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairment. (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

Emilio Di Maria

8

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

author name string

Alessandro Cocchella

1

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

Michela Malacarne

2

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

Francesca Forzano

3

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

Carmela Marciano

4

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

Mauro Pierluigi

5

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

Lucia Perroni

6

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

Francesca Faravelli

7

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

publication date

1 October 2010

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Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

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Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

153B

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Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

7

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

1342-1346

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

Human Ca2+/calmodulin-dependent phosphodiesterase PDE1A: novel splice variants, their specific expression, genomic organization, and chromosomal localization

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31107

21 January 2018

Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: further clinical and molecular delineation of del(2q32) syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31107

21 January 2018

Identifiers

10.1002/AJMG.B.31107

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 April 2018

http://europepmc.org/abstract/MED/20552675

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