(Q37608101)

21 August 2017

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title

Monosomy for the X chromosome (English)

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21 August 2017

Carolyn A Bondy

1

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21 August 2017

Clara Cheng

series ordinal

2

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21 August 2017

publication date

1 January 2009

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21 August 2017

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21 August 2017

volume

17

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21 August 2017

issue

5

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21 August 2017

page(s)

649-658

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Ullrich-Turner syndrome is not caused by haploinsufficiency of RPS4X

21 August 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10577-009-9052-Z

Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10577-009-9052-Z

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10577-009-9052-Z

The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome.

21 January 2018

1 reference

12 December 2020

X chromosome gene expression in human tissues: male and female comparisons.

1 reference

12 December 2020

X-inactivation profile reveals extensive variability in X-linked gene expression in females

1 reference

12 December 2020

Differential and correlation analyses of microarray gene expression data in the CEPH Utah families

1 reference

12 December 2020

Introduction to the study of pre- and postnatal growth in humans: a review

1 reference

12 December 2020

Zfx controls the self-renewal of embryonic and hematopoietic stem cells.

1 reference

12 December 2020

UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development

1 reference

12 December 2020

Application of microarrays to the analysis of the inactivation status of human X-linked genes expressed in lymphocytes

1 reference

12 December 2020

Zfx mutation results in small animal size and reduced germ cell number in male and female mice

1 reference

12 December 2020

Incidence and spectrum of chromosome abnormalities in spontaneous abortions: new insights from a 12-year study

1 reference

12 December 2020

Cognition and the sex chromosomes: studies in Turner syndrome

1 reference

12 December 2020

Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia

1 reference

12 December 2020

Transient homologous chromosome pairing marks the onset of X inactivation

1 reference

12 December 2020

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

1 reference

12 December 2020

Developmental analysis of cardiovascular system of 45,X fetuses with cystic hygroma.

1 reference

12 December 2020

Transient colocalization of X-inactivation centres accompanies the initiation of X inactivation.

1 reference

12 December 2020

KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS

1 reference

12 December 2020

Human DDX3Y, the Y-encoded isoform of RNA helicase DDX3, rescues a hamster temperature-sensitive ET24 mutant cell line with a DDX3X mutation

1 reference

12 December 2020

Sex-specific expression of the X-linked histone demethylase gene Jarid1c in brain

1 reference

12 December 2020

Maternal X Chromosome, Visceral Adiposity, and Lipid Profile

1 reference

12 December 2020

Functional equivalence of human X- and Y-encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndrome

1 reference

12 December 2020

Phenotypes Associated with SHOX Deficiency

1 reference

12 December 2020

Jugular lymphatic maldevelopment in Turner syndrome and trisomy 21: different anomalies leading to nuchal edema

1 reference

12 December 2020

A Turner syndrome neurocognitive phenotype maps to Xp22.3.

1 reference

12 December 2020

Relationship between the monosomy X phenotype and Y-linked ribosomal protein S4 (Rps4) in several species of mammals: a molecular evolutionary analysis of Rps4 homologs

1 reference

12 December 2020

Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines.

1 reference

12 December 2020

Dosage compensation of the active X chromosome in mammals

1 reference

12 December 2020

The X chromosome is organized into a gene-rich outer rim and an internal core containing silenced nongenic sequences

1 reference

12 December 2020

[Height in Turner's syndrome: correlation with parents' height]

1 reference

12 December 2020

1 reference

12 December 2020

The physical phenotype of girls and women with Turner syndrome is not X-imprinted.

1 reference

12 December 2020

Major vascular anomalies in Turner syndrome: prevalence and magnetic resonance angiographic features

1 reference

12 December 2020

Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner Syndrome

1 reference

12 December 2020

Genomic imprinting in Turner syndrome: effects on response to growth hormone and on risk of sensorineural hearing loss

1 reference

12 December 2020

Aortic dilatation and dissection in Turner syndrome.

1 reference

12 December 2020

The will-o'-the-wisp of genetics--hunting for the azoospermia factor gene

1 reference

12 December 2020

SHOX: growth, Léri-Weill and Turner syndromes

1 reference

12 December 2020

A stain upon the silence: genes escaping X inactivation

1 reference

12 December 2020

A novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced

1 reference

12 December 2020

A cross-species comparison of X-chromosome inactivation in Eutheria

1 reference

12 December 2020

Turner syndrome and haploinsufficiency

1 reference

12 December 2020

Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y

1 reference

12 December 2020

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

1 reference

12 December 2020

The DNA sequence of the human X chromosome

1 reference

12 December 2020

X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications

1 reference

12 December 2020

Large-scale population study of human cell lines indicates that dosage compensation is virtually complete

1 reference

12 December 2020

Possible role of imprinting in the Turner phenotype

1 reference

12 December 2020

Prevalence, incidence, diagnostic delay, and mortality in Turner syndrome.

1 reference

12 December 2020

FAM/USP9x, a deubiquitinating enzyme essential for TGFbeta signaling, controls Smad4 monoubiquitination

1 reference

12 December 2020

Growth hormone treatment of non-growth hormone-deficient growth disorders

1 reference

12 December 2020

X-monosomy effects on visuospatial attention in mice: a candidate gene and implications for Turner syndrome and attention deficit hyperactivity disorder.

1 reference

12 December 2020

The human pseudoautosomal regions: a review for genetic epidemiologists

1 reference

12 December 2020

Sterility associated with an XO karyotype in a miniature horse mare

1 reference

12 December 2020

10.1007/S10577-009-9052-Z

Identifiers

DOI

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21 August 2017

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