(Q35899367)

11 August 2017

Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe (English)

1 reference

11 August 2017

0 references

Babak Khoshnood

8

0 references

Elizabeth S Draper

object named as

Elizabeth Draper

series ordinal

16

0 references

Marian Bakker

series ordinal

13

object named as

Marian Bakker

1 reference

11 August 2017

6

Vera Nelen

1 reference

11 August 2017

15

Marie-Claude Addor

1 reference

11 August 2017

5

Martin Haeusler

1 reference

11 August 2017

12

Elisa Calzolari

1 reference

11 August 2017

11

Carmel Mullaney

1 reference

11 August 2017

7

Ester Garne

1 reference

11 August 2017

4

Ruth Greenlees

1 reference

11 August 2017

17

Judith Rankin

1 reference

11 August 2017

2

Helen Dolk

1 reference

11 August 2017

9

Berenice Doray

1 reference

11 August 2017

10

Anke Rissmann

1 reference

11 August 2017

18

David Tucker

1 reference

11 August 2017

1

Diana Wellesley

1 reference

11 August 2017

Patricia A Boyd

3

1 reference

PMC publication ID

3330224

11 August 2017

Joaquin Salvador

series ordinal

14

1 reference

11 August 2017

11 January 2012

1 reference

European Journal of Human Genetics

11 August 2017

1 reference

11 August 2017

20

1 reference

11 August 2017

5

1 reference

11 August 2017

521-526

1 reference

The prevalence of congenital anomalies in Europe

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Prenatal diagnosis for chromosome abnormalities: past, present and future

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Inherited structural cytogenetic abnormalities detected incidentally in fetuses diagnosed prenatally: frequency, parental-age associations, sex-ratio trends, and comparisons with rates of mutants

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Extra structurally abnormal chromosomes (ESAC) detected at amniocentesis: frequency in approximately 75,000 prenatal cytogenetic diagnoses and associations with maternal and paternal age

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Genetic disorders in children and young adults: a population study

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Frequency of births with potentially avoidable serious chromosomal anomalies in EEC countries, 1979-1982.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Incidence of chromosome aberrations among 11 148 newborn children

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

The incidence and etiology of sex chromosome abnormalities in man

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

The European Perinatal Health Report: comparing the health and care of pregnant women and newborn babies in Europe

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

A total population study of diagnosed chromosome abnormalities in Queensland, Australia

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Chromosomal abnormality rates at amniocentesis and in live-born infants

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330224

Mortality risks in patients with constitutional autosomal chromosome deletions in Britain: a cohort study

24 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2011.246

Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited

21 January 2018

1 reference

12 December 2020

The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey

1 reference

12 December 2020

Supernumerary marker chromosomes detected in 100,000 prenatal diagnoses: molecular cytogenetic studies and clinical significance

1 reference

12 December 2020

Patterns of chromosomal deletions identified by a birth defects registry, Hawaii, 1986-2003

1 reference

12 December 2020

Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe

1 reference

12 December 2020

Prenatal detection of rare chromosomal autosomal abnormalities in Europe

1 reference

12 December 2020

Epidemiology of triploidy in a population-based birth defects registry, Hawaii, 1986-1999

1 reference

12 December 2020

Chromosomal Abnormalities in the Human Population: Estimation of Rates Based on New Haven Newborn Study

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.2011.246

1 reference

11 August 2017

1 reference

PMC publication ID

3330224

11 August 2017

PubMed publication ID

22234154

1 reference

PMC publication ID

3330224