about
Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosomeRecent advances in prenatal genetic screening and testingReturn of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) NetworkCryptic subtelomeric rearrangements and X chromosome mosaicism: a study of 565 apparently normal individuals with fluorescent in situ hybridization.Chromosome abnormalities in Indonesian patients with short stature.Somatic genome variations in health and diseaseOntogenetic variation of the human genome.Possible influence of menstrual cycle on lymphocyte X chromosome mosaicismHuman adipose stromal cells (ASC) for the regeneration of injured cartilage display genetic stability after in vitro culture expansion.The proportion of diploid 46,XX cells increases with time in women with Turner syndrome--a 10-year follow-up study.Non-invasive prenatal testing for sex chromosome abnormalities: a source of confusionIncidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing PopulationAbnormal plasma DNA profiles in early ovarian cancer using a non-invasive prenatal testing platform: implications for cancer screening.Genetic considerations in the patient with Turner syndrome--45,X with or without mosaicism.Chromosomal mosaicism goes global.Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPT.Follow-up of multiple aneuploidies and single monosomies detected by noninvasive prenatal testing: implications for management and counseling.GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny.Human embryonic stem cells and genomic instability.X chromosome aneuploidy in the Alzheimer's disease brain.Demographic associations for autoantibodies in disease-free individuals of a European population.Non-invasive prenatal testing for aneuploidy: current status and future prospects.Detecting somatic mosaicism: considerations and clinical implications.Clinical implementation of NIPT - technical and biological challenges.Cell-free DNA screening and sex chromosome aneuploidies.Noninvasive prenatal testing for aneuploidy using cell-free DNA - New implications for maternal health.Identification of a novel 15.5 kb SHOX deletion associated with marked intrafamilial phenotypic variability and analysis of its molecular origin.A time stamp comparative analysis of frequent chromosomal abnormalities in Romanian patients.Strong associations between chromosomal aberrations in blood lymphocytes and the risk of urothelial and squamous cell carcinoma of the bladder.Y chromosome aberration in a patient with cloacal-bladder exstrophy-epispadias complex: an unusual finding.In silico size selection is effective in reducing false positive NIPS cases of monosomy X that are due to maternal mosaic monosomy X.Cherchez la femme: maternal incidental findings can explain discordant prenatal cell-free DNA sequencing results.Sex chromosome aneuploidy detection by noninvasive prenatal testing: helpful or hazardous?The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.Current best practice in the management of Turner syndrome.Non-invasive risk assessment of fetal sex chromosome aneuploidy through directed analysis and incorporation of fetal fraction.Sex chromosome loss may represent a disease-associated clonal population in chronic lymphocytic leukemia
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
X chromosome loss and ageing.
@en
type
label
X chromosome loss and ageing.
@en
prefLabel
X chromosome loss and ageing.
@en
P2093
P356
P1476
X chromosome loss and ageing.
@en
P2093
P304
P356
10.1159/000098184
P577
2007-01-01T00:00:00Z