(Q34514946)

2 August 2017

Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancy (English)

1 reference

2 August 2017

2

Maria Loane

0 references

Babak Khoshnood

object named as

Babak Khoshnood

series ordinal

4

0 references

Ester Garne

series ordinal

3

object named as

Ester Garne

1 reference

2 August 2017

5

Helen Dolk

1 reference

2 August 2017

Patricia Anne Boyd

1

1 reference

PubMed ID

20736977

2 August 2017

EUROCAT working group

series ordinal

6

1 reference

2 August 2017

25 August 2010

1 reference

European Journal of Human Genetics

2 August 2017

1 reference

2 August 2017

19

1 reference

2 August 2017

2

1 reference

2 August 2017

231-234

1 reference

https://scigraph.springernature.com/pub.10.1038/ejhg.2010.148

2 August 2017

0 references

cites work

Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025783

Triple X syndrome: a review of the literature

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025783

Noninvasive prenatal detection of fetal chromosomal aneuploidies by maternal plasma nucleic acid analysis: a review of the current state of the art.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025783

Impact of a new national screening policy for Down's syndrome in Denmark: population based cohort study.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025783

Survey of prenatal screening policies in Europe for structural malformations and chromosome anomalies, and their impact on detection and termination rates for neural tube defects and Down's syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025783

Is the prevalence of Klinefelter syndrome increasing?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025783

What parents are told after prenatal diagnosis of a sex chromosome abnormality: interview and questionnaire study

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025783

Long-term outcome in children of sex chromosome abnormalities

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025783

47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025783

A cytogenetic survey of 11,680 newborn infants

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025783

Incidence of chromosome aberrations among 11 148 newborn children

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025783

Termination of pregnancy for fetal anomaly after 23 weeks of gestation: a European register-based study

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2010.148

Outcomes of pregnancies diagnosed with Klinefelter syndrome: the possible influence of health professionals†

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2010.148

Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses

21 January 2018

1 reference

12 December 2020

Genetic counseling for sex chromosome abnormalities

1 reference

12 December 2020

Pregnancy outcome and prenatal diagnosis of sex chromosome abnormalities in Hawaii, 1986-1999

1 reference

12 December 2020

Prenatal diagnosis and management of sex chromosome aneuploidy: a report on 98 cases

1 reference

12 December 2020

Factors influencing parental decision making in prenatal diagnosis of sex chromosome aneuploidy

1 reference

12 December 2020

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities

1 reference

12 December 2020

Identifiers

DOI

10.1038/EJHG.2010.148

1 reference

2 August 2017

1 reference

2 August 2017

1 reference

PubMed ID

20736977