Molecular cytogenetics and cytogenomics of brain diseases.
about
Potential epigenetic mechanism(s) associated with the persistence of psychoneurological symptoms in women receiving chemotherapy for breast cancer: a hypothesisDiversity of sex chromosome abnormalities in a cohort of 95 Indonesian patients with monosomy XAccurate distinction of pathogenic from benign CNVs in mental retardation.Human interphase chromosomes: a review of available molecular cytogenetic technologies.Somatic genome variations in health and diseaseSomatic genomic variations in extra-embryonic tissuesOntogenetic variation of the human genome.Molecular cytogenetic diagnosis and somatic genome variations.Genomic and epigenomic instability, fragile sites, schizophrenia and autism.Increased frequency of micronuclei in adults with a history of childhood sexual abuse: a discordant monozygotic twin study.In silico molecular cytogenetics: a bioinformatic approach to prioritization of candidate genes and copy number variations for basic and clinical genome research.Assessment of copy number variations in the brain genome of schizophrenia patients.Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsy.Single cell genomics of the brain: focus on neuronal diversity and neuropsychiatric diseases.3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances.Chromosomal mosaicism goes global.GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny.X chromosome aneuploidy in the Alzheimer's disease brain.An interstitial 20q11.21 microdeletion causing mild intellectual disability and facial dysmorphisms.An interstitial deletion at 10q26.2q26.3.Somatic mosaicism in cases with small supernumerary marker chromosomes.Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the diseaseRetrotransposing Gremlins May Disrupt Our Brain's Genomes.Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies.Behavioral Variability and Somatic Mosaicism: A Cytogenomic Hypothesis.Yuri B. Yurov (1951-2017).
P2860
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P2860
Molecular cytogenetics and cytogenomics of brain diseases.
description
2008 nî lūn-bûn
@nan
2008 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Molecular cytogenetics and cytogenomics of brain diseases.
@ast
Molecular cytogenetics and cytogenomics of brain diseases.
@en
type
label
Molecular cytogenetics and cytogenomics of brain diseases.
@ast
Molecular cytogenetics and cytogenomics of brain diseases.
@en
prefLabel
Molecular cytogenetics and cytogenomics of brain diseases.
@ast
Molecular cytogenetics and cytogenomics of brain diseases.
@en
P2093
P2860
P1433
P1476
Molecular cytogenetics and cytogenomics of brain diseases.
@en
P2093
I Y Iourov
S G Vorsanova
P2860
P304
P356
10.2174/138920208786241216
P577
2008-11-01T00:00:00Z