(Q44246703)

1 December 2017

The contribution of chromosomal abnormalities to congenital heart defects: a population-based study (English)

1 reference

1 December 2017

2

Sonja A Rasmussen

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Tiffany Riehle-Colarusso

series ordinal

4

object named as

Tiffany Riehle-Colarusso

1 reference

1 December 2017

5

Christa L Martin

1 reference

1 December 2017

8

Adolfo Correa

1 reference

1 December 2017

3

Lorenzo D Botto

1 reference

1 December 2017

Robert J Hartman

1

1 reference

PubMed ID

21728077

1 December 2017

Janet D Cragan

series ordinal

6

1 reference

PubMed ID

21728077

1 December 2017

Mikyong Shin

series ordinal

7

1 reference

1 December 2017

5 July 2011

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1 December 2017

1 reference

1 December 2017

32

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1 December 2017

8

1 reference

1 December 2017

1147-1157

1 reference

https://scigraph.springernature.com/pub.10.1007/s00246-011-0034-5

1 December 2017

0 references

cites work

Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Including prenatal diagnoses in birth defects monitoring: Experience of the Metropolitan Atlanta Congenital Defects Program.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Descriptive epidemiology of congenital heart disease in Northern England.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Syndromes and malformations associated with congenital heart disease in a population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

The epidemiology of cardiovascular defects, part 2: a study based on data from three large registries of congenital malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

The incidence of congenital heart defects in the first year of life

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Chromosomal abnormalities among children born with conotruncal cardiac defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Congenital heart disease and genetic syndromes: specific correlation between cardiac phenotype and genotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Double outlet right ventricle: aetiologies and associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pedia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Epidemiology of major congenital heart defects in Sweden, 1981-1986

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Prevalence of congenital heart defects in metropolitan Atlanta, 1998-2005.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Improving the quality of surveillance data on congenital heart defects in the metropolitan Atlanta congenital defects program

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Risk factors in congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

The importance of nomenclature for congenital cardiac disease: implications for research and evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Associations between chromosomal anomalies and congenital heart defects: a database search.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Racial differences in infant mortality attributable to birth defects in the United States, 1989-2002.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-011-0034-5

Unexpected survival in a case of prenatally diagnosed non-mosaic trisomy 22: Clinical report and review of the natural history

21 January 2018

1 reference

12 December 2020

New trends in chromosomal investigation in children with cardiovascular malformations

1 reference

12 December 2020

Hospital stays, hospital charges, and in-hospital deaths among infants with selected birth defects--United States, 2003.

1 reference

12 December 2020

Infant mortality statistics from the 2005 period linked birth/infant death data set.

1 reference

12 December 2020

Chromosome abnormalities in congenital heart disease

1 reference

12 December 2020

Estimates of the economic costs of birth defects

1 reference

12 December 2020

Reporting birth defects surveillance data 1968-2003.

1 reference

12 December 2020

Temporal variability in birth prevalence of congenital heart defects as recorded by a general birth defects registry

1 reference

12 December 2020

Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study

1 reference

12 December 2020

Enhanced detection of clinically relevant genomic imbalances using a targeted plus whole genome oligonucleotide microarray

1 reference

12 December 2020

Congenital cardiovascular malformations (CCVM) and structural chromosome abnormalities: a report of 9 cases and literature review

1 reference

12 December 2020

Anomalies in Down syndrome individuals in a large population-based registry

1 reference

12 December 2020

10.1007/S00246-011-0034-5

Identifiers

DOI

1 reference

1 December 2017

1 reference

PubMed ID

21728077