(Q50304592)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23061379%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

title

Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH (English)

1 reference

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10 March 2020

1 reference

10

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10 March 2020

Valérie Malan

13

1 reference

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10 March 2020

Marlene Rio

1

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10 March 2020

Jean-Paul Bonnefont

9

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10 March 2020

author name string

G Royer

2

1 reference

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10 March 2020

S Gobin

3

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10 March 2020

M C de Blois

4

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10 March 2020

C Ozilou

5

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10 March 2020

A Bernheim

6

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10 March 2020

M Nizon

7

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10 March 2020

A Munnich

8

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10 March 2020

M Vekemans

11

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10 March 2020

C Turleau

12

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10 March 2020

publication date

4 November 2012

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10 March 2020

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10 March 2020

volume

84

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10 March 2020

issue

1

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10 March 2020

page(s)

31-36

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Monozygotic twins with 22q11 deletion and discordant phenotypes

10 March 2020

cites work

1 reference

Mechanisms for differences in monozygous twins

21 January 2018

1 reference

Epigenetic differences arise during the lifetime of monozygotic twins

21 January 2018

1 reference

DNA methylation profiles in monozygotic and dizygotic twins.

21 January 2018

1 reference

Phenotypic discordance in a pair of monozygotic twins with Huntington's disease

21 January 2018

1 reference

Spinocerebellar ataxia in monozygotic twins

21 January 2018

1 reference

Some causes of genotypic and phenotypic discordance in monozygotic twin pairs

21 January 2018

1 reference

Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

21 January 2018

1 reference

Ontogenetic de novo copy number variations (CNVs) as a source of genetic individuality: studies on two families with MZD twins for schizophrenia

21 January 2018

1 reference

Intragenic breakpoints localized by array CGH in a t(2;6) familial translocation

21 January 2018

1 reference

MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletions.

21 January 2018

1 reference

Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia

21 January 2018

1 reference

Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism

21 January 2018

1 reference

Neuroligins 3 and 4X interact with syntrophin-gamma2, and the interactions are affected by autism-related mutations

21 January 2018

1 reference

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 January 2018

1 reference

Disorder-associated mutations lead to functional inactivation of neuroligins

21 January 2018

1 reference

Characterization of the solution structure of a neuroligin/beta-neurexin complex

21 January 2018

1 reference

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

21 January 2018

1 reference

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

21 January 2018

1 reference

Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders

21 January 2018

1 reference

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

21 January 2018

1 reference

The obesity gene, TMEM18, is of ancient origin, found in majority of neuronal cells in all major brain regions and associated with obesity in severely obese children

21 January 2018

1 reference

Unexplained autism is frequently associated with low-level mosaic aneuploidy.

21 January 2018

1 reference

Inducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombination

21 January 2018

1 reference

A copy number variation morbidity map of developmental delay

21 January 2018

1 reference

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/CGE.12036

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23061379%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

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