(Q24306560)

1

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Richard Schroer

2

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Jin Yan

3

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Wenjia Song

4

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Chunmei Yang

5

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Anke Bockholt

6

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Cindy Skinner

8

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Charles E Schwartz

9

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Steve S Sommer

Absence of MeCP2 mutations in patients from the South Carolina autism project

10

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language of work or name

English

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publication date

27 November 2006

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published in

Neuroscience Letters

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volume

409

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issue

1

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page(s)

10-3

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Autism and maternally derived aberrations of chromosome 15q.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Analysis of the human neurexin genes: alternative splicing and the generation of protein diversity

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Structure and evolution of neurexin genes: insight into the mechanism of alternative splicing

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Autism and tuberous sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

The Pre-Linguistic Autism Diagnostic Observation Schedule

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

The role of age at assessment, developmental level, and test in the stability of intelligence scores in young autistic children.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS)

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

CCG repeats in cDNAs from human brain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Neuroligin 1: a splice site-specific ligand for beta-neurexins

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Cartography of neurexins: more than 1000 isoforms generated by alternative splicing and expressed in distinct subsets of neurons.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Neurexins: three genes and 1001 products

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

PDZ domains in synapse assembly and signalling

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Neurexin mediates the assembly of presynaptic terminals

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

A new method for predicting signal sequence cleavage sites

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Scanning by DOVAM-S detects all unique sequence changes in blinded analyses: evidence that the scanning conditions are generic

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

Detection of virtually all mutations-SSCP (DOVAM-S): a rapid method for mutation scanning with virtually 100% sensitivity

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEULET.2006.08.017

7 January 2021

10.1016/J.NEULET.2006.08.017

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

17034946

1 reference

Consolidated OpenCitations Corpus – April 2017