(Q51930226)

17 April 2018

title

A de novo 1.9-Mb interstitial deletion of 3q13.2q13.31 in a girl with dysmorphic features, muscle hypotonia, and developmental delay. (English)

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17 April 2018

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Keiko Shimojima

1

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17 April 2018

Kayoko Saito

series ordinal

2

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17 April 2018

Toshiyuki Yamamoto

series ordinal

3

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17 April 2018

language of work or name

English

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publication date

1 August 2009

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17 April 2018

American Journal of Medical Genetics

published in

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17 April 2018

volume

149A

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17 April 2018

issue

8

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17 April 2018

page(s)

1818-1822

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17 April 2018

A targeted mutation of the D3 dopamine receptor gene is associated with hyperactivity in mice

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32963

Dopaminergic mechanism of reward-related incentive learning: focus on the dopamine D(3) receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32963

Boy with a chromosome del (3)(q12q23) and blepharophimosis syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32963

A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32963

From dopaminergic genes to psychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32963

BOC, an Ig superfamily member, associates with CDO to positively regulate myogenic differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32963

Promyogenic members of the Ig and cadherin families associate to positively regulate differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32963

Developmental characteristics of very low-birthweight infants at 18 months' corrected age according to birthweight.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32963

Patient with novel interstitial deletion of chromosome 3q13.1q13.3 and agenesis of the corpus callosum

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32963

Two patients with atypical interstitial deletions of 8p23.1: mapping of phenotypical traits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32963

Congenital arhinia: molecular-genetic analysis of five patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.32963

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.32963

1 reference

17 April 2018

1 reference

17 April 2018