Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy
about
Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking dupliconsThe comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Genomic imprinting disorders in humans: a mini-reviewGenetic mapping of putative Chrna7 and Luzp2 neuronal transcriptional enhancers due to impact of a transgene-insertion and 6.8 Mb deletion in a mouse model of Prader-Willi and Angelman syndromes.Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in miceGenetics of Prader-Willi syndrome and Prader-Will-Like syndromePrader-Willi syndrome mental health research strategy workshop proceedings: the state of the science and future directionsThe 15q11.2 BP1-BP2 microdeletion syndrome: a reviewFunctional characterization of NIPA2, a selective Mg2+ transporterCyfip1 Regulates Presynaptic Activity during DevelopmentNIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporterFrench database of children and adolescents with Prader-Willi syndrome.Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint regionGenome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsiesCauses of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality surveyExpression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndromePerceptions of body image by persons with Prader-Willi syndrome and their parents.Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalitiesClinical management of behavioral characteristics of Prader-Willi syndrome.High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosagePrader-Willi Syndrome: Obesity due to Genomic Imprinting.Systematic review of the clinical and genetic aspects of Prader-Willi syndrome.Psychiatric illness and intellectual disability in the Prader-Willi syndrome with different molecular defects--a meta analysis.Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum DisordersIncreased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTORPrader-Willi syndrome: A primer for clinicians.Prader-Willi syndrome and autism spectrum disorders: an evolving story.Importance of reward and prefrontal circuitry in hunger and satiety: Prader-Willi syndrome vs simple obesity.Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.The neuroanatomy of genetic subtype differences in Prader-Willi syndromeMethylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.Lack of Postprandial Peak in Brain-Derived Neurotrophic Factor in Adults with Prader-Willi Syndrome.Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.Leisure activities in Prader-Wili syndrome: implications for health, cognition and adaptive functioningParental origin impairment of synaptic functions and behaviors in cytoplasmic FMRP interacting protein 1 (Cyfip1) deficient miceMicroarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlationsA twin sibling with Prader-Willi syndrome caused by type 2 microdeletion following assisted reproductive technology: A case report.Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome.Behavioral profile of adults with Prader-Willi syndrome: correlations with individual and environmental variables.A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease.
P2860
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P2860
Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy
description
2004 nî lūn-bûn
@nan
2004 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մարտին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Behavioral differences among s ...... I deletion and maternal disomy
@ast
Behavioral differences among s ...... I deletion and maternal disomy
@en
Behavioral differences among s ...... I deletion and maternal disomy
@nl
type
label
Behavioral differences among s ...... I deletion and maternal disomy
@ast
Behavioral differences among s ...... I deletion and maternal disomy
@en
Behavioral differences among s ...... I deletion and maternal disomy
@nl
prefLabel
Behavioral differences among s ...... I deletion and maternal disomy
@ast
Behavioral differences among s ...... I deletion and maternal disomy
@en
Behavioral differences among s ...... I deletion and maternal disomy
@nl
P2093
P3181
P356
P1433
P1476
Behavioral differences among s ...... I deletion and maternal disomy
@en
P2093
Douglas C Bittel
Merlin G Butler
Nataliya Kibiryeva
Travis Thompson
Zohreh Talebizadeh
P304
P3181
P356
10.1542/PEDS.113.3.565
P407
P433
P577
2004-03-01T00:00:00Z