(Q24316311)

corpus callosum morphogenesis

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Peter Nürnberg

16

0 references

Christian Kubisch

18

Christian Kubisch

0 references

Lina Basel-Vanagaite

1

Lina Basel-Vanagaite

0 references

Metsada Pasmanik-Chor

15

Metsada Pasmanik-Chor

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Miquel Raspall-Chaure

Miquel Raspall-Chaure

4

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Marta Vila-Pueyo

Marta Vila-Pueyo

7

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Holger Thiele

9

Holger Thiele

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Mordechai Shohat

19

Mordechai Shohat

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author name string

Tova Hershkovitz

2

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Eli Heyman

3

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Naseebullah Kakar

5

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Pola Smirin-Yosef

6

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Liora Kornreich

8

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Harald Bode

10

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Irina Lagovsky

11

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Dvir Dahary

12

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Ami Haviv

13

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Monika Weisz Hubshman

14

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Doron Gothelf

17

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Alfons Macaya

20

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Guntram Borck

American Journal of Human Genetics

21

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language of work or name

English

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publication date

5 September 2013

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published in

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volume

93

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issue

3

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page(s)

524-9

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cites work

A novel giant peroxisomal superoxide dismutase motif-containing protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Szt2, a novel gene for seizure threshold in mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Exome sequencing as a tool for Mendelian disease gene discovery

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Molecular bases and clinical spectrum of early infantile epileptic encephalopathies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Clinical review of genetic epileptic encephalopathies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Rare copy number variants are an important cause of epileptic encephalopathies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Ohtahara syndrome with emphasis on recent genetic discovery.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Clinical evaluation and diagnosis of severe epilepsy syndromes of early childhood

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Effects of seizures on developmental processes in the immature brain

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Basic science behind the catastrophic epilepsies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

The neurobiology and consequences of epilepsy in the developing brain

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

HomozygosityMapper--an interactive approach to homozygosity mapping

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

MRI of the brain in the Cohen syndrome: a relatively large corpus callosum in patients with mental retardation and microcephaly

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Developmental anomalies of the medial septal area: possible implication for limbic epileptogenesis.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Thick fetal corpus callosum: an ominous sign?

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

A patient with the syndrome of megalencephaly, mega corpus callosum and complete lack of motor development.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndrome

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769928

10.1016/J.AJHG.2013.07.005

29 November 2018

Identifiers

DOI

1 reference

1 reference

1 reference

PubMed publication ID

23932106

1 reference