(Q57719906)

Renata Rizzo

4

0 references

Marco Fichera

Marco Fichera

2

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Orazio Palumbo

Orazio Palumbo

1

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Massimo Carella

Massimo Carella

7

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author name string

Elisabetta Mazzolla

5

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Donatella Maria Cocuzza

6

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Teresa Mattina

American Journal of Medical Genetics

8

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language of work or name

English

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publication date

23 January 2014

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published in

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volume

164

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issue

3

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page(s)

828-833

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cites work

Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

Tbr1 regulates differentiation of the preplate and layer 6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

Transcription factors in glutamatergic neurogenesis: conserved programs in neocortex, cerebellum, and adult hippocampus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

The T-box brain 1 (Tbr1) transcription factor inhibits astrocyte formation in the olfactory bulb and regulates neural stem cell fate.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

Polymicrogyria and absence of pineal gland due to PAX6 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

An emerging phenotype of interstitial 15q25.2 microdeletions: Clinical report and review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

A novel deletion in 2q24.1q24.2 in a girl with mental retardation and generalized hypotonia: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363

Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 Microdeletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36363