Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1755-8166
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
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
- Urheber
-
Xu, Fang
Li, Lun
Schulz, Vincent P.
Gallagher, Patrick G.
Xiang, Bixia
Zhao, Hongyu
Li, Peining
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/1755-8166-7-4
- URN
-
urn:nbn:de:101:1-2021082920350755476733
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:30 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Xu, Fang
- Li, Lun
- Schulz, Vincent P.
- Gallagher, Patrick G.
- Xiang, Bixia
- Zhao, Hongyu
- Li, Peining
- SpringerLink (Online service)
Ähnliche Objekte (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
Genomic imbalances defining novel intellectual disability associated loci
Identification and characterization of mechanisms underlying intellectual disability
Calcium channelopathies and intellectual disability: a systematic review
Syndromic intellectual disability : genotypes and phenotypes in six patients
Meeting emotional needs in intellectual disability : the developmental approach
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
Genomic imbalances defining novel intellectual disability associated loci
Identification and characterization of mechanisms underlying intellectual disability
Calcium channelopathies and intellectual disability: a systematic review
Syndromic intellectual disability : genotypes and phenotypes in six patients
Meeting emotional needs in intellectual disability : the developmental approach
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
Genomic imbalances defining novel intellectual disability associated loci
Identification and characterization of mechanisms underlying intellectual disability
Calcium channelopathies and intellectual disability: a systematic review
Syndromic intellectual disability : genotypes and phenotypes in six patients
Meeting emotional needs in intellectual disability : the developmental approach
Biallelic variants in KIF14 cause intellectual disability with microcephaly