Clinical significance of the parental origin of the X chromosome in turner syndrome.
about
Child health, developmental plasticity, and epigenetic programmingDiversity of sex chromosome abnormalities in a cohort of 95 Indonesian patients with monosomy X[Growth hormone treatment inTurner syndrome: data and reflections].Sex dependent imprinting effects on complex traits in mice.Analysis of expressed SNPs identifies variable extents of expression from the human inactive X chromosome.At Term, XmO and XpO Mouse Placentas Show Differences in Glucose Metabolism in the Trophectoderm-Derived Outer ZoneChromosome imbalance as a driver of sex disparity in disease.Turner Syndrome Genotype and phenotype and their effect on presenting features and timing of DiagnosisNo influence of parental origin of intact X chromosome and/or Y chromosome sequences on three-year height response to growth hormone therapy in Turner syndrome.Turner syndrome and sexual differentiation of the brain: implications for understanding male-biased neurodevelopmental disordersGenomic imprinting effects on cognitive and social abilities in prepubertal girls with Turner syndromeTurner syndrome and the evolution of human sexual dimorphismEffect of the parental origin of the X-chromosome on the clinical features, associated complications, the two-year-response to growth hormone (rhGH) and the biochemical profile in patients with turner syndrome.Genomic imprinting effects of the X chromosome on brain morphology.Pulmonary alveolar proteinosis caused by deletion of the GM-CSFRalpha gene in the X chromosome pseudoautosomal region 1.Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.Early human embryos are naturally aneuploid-can that be corrected?Insulin resistance in adolescents with Turner syndrome is comparable to obese peers, but the overall metabolic risk is lower due to unknown mechanism.Prepubertal ultra-low-dose estrogen therapy is associated with healthier lipid profile than conventional estrogen replacement for pubertal induction in adolescent girls with Turner syndrome: preliminary results.X chromosome parental origin and aortic stiffness in turner syndrome.Preliminary Evidence for Aortopathy and an X-Linked Parent-of-Origin Effect on Aortic Valve Malformation in a Mouse Model of Turner Syndrome.The Natural History of Metabolic Comorbidities in Turner Syndrome from Childhood to Early Adulthood: Comparison between 45,X Monosomy and Other Karyotypes.Epigenetics in Turner syndrome.
P2860
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P2860
Clinical significance of the parental origin of the X chromosome in turner syndrome.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Clinical significance of the parental origin of the X chromosome in turner syndrome.
@en
Clinical significance of the parental origin of the X chromosome in turner syndrome.
@nl
type
label
Clinical significance of the parental origin of the X chromosome in turner syndrome.
@en
Clinical significance of the parental origin of the X chromosome in turner syndrome.
@nl
prefLabel
Clinical significance of the parental origin of the X chromosome in turner syndrome.
@en
Clinical significance of the parental origin of the X chromosome in turner syndrome.
@nl
P2093
P356
P1476
Clinical significance of the parental origin of the X chromosome in turner syndrome.
@en
P2093
Alessandra Vottero
Aneta Gawlik
Atilla Buyukgebiz
Fuad Fares
Liora Sagi
Lucia Ghizzoni
Nehama Zuckerman-Levin
Oshrat Baruch
Osnat Admoni
Tzvi Bistritzer
P304
P356
10.1210/JC.2006-0158
P407
P577
2006-12-27T00:00:00Z