Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1755-8166

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability ; volume:7 ; number:1 ; day:10 ; month:1 ; year:2014 ; pages:1-13 ; date:12.2014
Molecular cytogenetics ; 7, Heft 1 (10.1.2014), 1-13, 12.2014

Creator: Xu, Fang
Li, Lun
Schulz, Vincent P.
Gallagher, Patrick G.
Xiang, Bixia
Zhao, Hongyu
Li, Peining

Contributor: SpringerLink (Online service)

DOI: 10.1186/1755-8166-7-4

URN: urn:nbn:de:101:1-2021082920350755476733

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:30 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Xu, Fang
Li, Lun
Schulz, Vincent P.
Gallagher, Patrick G.
Xiang, Bixia
Zhao, Hongyu
Li, Peining
SpringerLink (Online service)

Other Objects (12)

Autosomal dominant intellectual disability

Genetics of autosomal recessive intellectual disability

Intellectual disability and nutrition‐related health

Bioinformatic analysis of xenobiotic reactive metabolite target proteins and their interacting partners

Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures

Identification and characterization of mechanisms underlying intellectual disability

Genomic imbalances defining novel intellectual disability associated loci

Calcium channelopathies and intellectual disability: a systematic review

Meeting emotional needs in intellectual disability : the developmental approach

Hochschulschrift

Syndromic intellectual disability : genotypes and phenotypes in six patients

Biallelic variants in KIF14 cause intellectual disability with microcephaly

"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements

Autosomal dominant intellectual disability

Genetics of autosomal recessive intellectual disability

Intellectual disability and nutrition‐related health

Bioinformatic analysis of xenobiotic reactive metabolite target proteins and their interacting partners

Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures

Identification and characterization of mechanisms underlying intellectual disability

Genomic imbalances defining novel intellectual disability associated loci

Calcium channelopathies and intellectual disability: a systematic review

Meeting emotional needs in intellectual disability : the developmental approach

Hochschulschrift

Syndromic intellectual disability : genotypes and phenotypes in six patients

Biallelic variants in KIF14 cause intellectual disability with microcephaly

"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements

Autosomal dominant intellectual disability

Genetics of autosomal recessive intellectual disability

Intellectual disability and nutrition‐related health

Bioinformatic analysis of xenobiotic reactive metabolite target proteins and their interacting partners

Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures

Identification and characterization of mechanisms underlying intellectual disability

Genomic imbalances defining novel intellectual disability associated loci

Calcium channelopathies and intellectual disability: a systematic review

Meeting emotional needs in intellectual disability : the developmental approach

Hochschulschrift

Syndromic intellectual disability : genotypes and phenotypes in six patients

Biallelic variants in KIF14 cause intellectual disability with microcephaly

"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Autosomal dominant intellectual disability

Genetics of autosomal recessive intellectual disability

Intellectual disability and nutrition‐related health

Bioinformatic analysis of xenobiotic reactive metabolite target proteins and their interacting partners

Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures

Identification and characterization of mechanisms underlying intellectual disability

Genomic imbalances defining novel intellectual disability associated loci

Calcium channelopathies and intellectual disability: a systematic review

Meeting emotional needs in intellectual disability : the developmental approach

Syndromic intellectual disability : genotypes and phenotypes in six patients

Biallelic variants in KIF14 cause intellectual disability with microcephaly

"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements

Autosomal dominant intellectual disability

Genetics of autosomal recessive intellectual disability

Intellectual disability and nutrition‐related health

Bioinformatic analysis of xenobiotic reactive metabolite target proteins and their interacting partners

Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures

Identification and characterization of mechanisms underlying intellectual disability

Genomic imbalances defining novel intellectual disability associated loci

Calcium channelopathies and intellectual disability: a systematic review

Meeting emotional needs in intellectual disability : the developmental approach

Syndromic intellectual disability : genotypes and phenotypes in six patients

Biallelic variants in KIF14 cause intellectual disability with microcephaly

"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements

Autosomal dominant intellectual disability

Genetics of autosomal recessive intellectual disability

Intellectual disability and nutrition‐related health

Bioinformatic analysis of xenobiotic reactive metabolite target proteins and their interacting partners

Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures

Identification and characterization of mechanisms underlying intellectual disability

Genomic imbalances defining novel intellectual disability associated loci

Calcium channelopathies and intellectual disability: a systematic review

Meeting emotional needs in intellectual disability : the developmental approach

Syndromic intellectual disability : genotypes and phenotypes in six patients

Biallelic variants in KIF14 cause intellectual disability with microcephaly

"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements

Related objects

Reset password