Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease (Q57828177)

7

0 references

author name string

Ashleigh A Richards

1

0 references

Lane Jaeckle Santos

2

0 references

Haley A Nichols

3

0 references

Bill P Crider

4

0 references

Frederick F Elder

5

0 references

Natalie S Hauser

https://scigraph.springernature.com/pub.10.1203/pdr.0b013e31818095d0

6

0 references

language of work or name

English

0 references

publication date

October 2008

0 references

published in

Pediatric Research

0 references

volume

64

0 references

issue

4

0 references

page(s)

358-363

0 references

exact match

0 references

cites work

The incidence of congenital heart disease

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Causes of congenital heart diseases: old and new modes, mechanisms, and models

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Genetic basis of congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

The genetic contribution to congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

The genetics of cardiac birth defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Human cytogenetics: 46 chromosomes, 46 years and counting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Copy number variation in the human genome and its implications for cardiovascular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

A faster circular binary segmentation algorithm for the analysis of array CGH data

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Partial trisomy 2q: report of a patient with dup (2)(q33.1q35).

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

DiGeorge syndrome: the use of model organisms to dissect complex genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Kousseff syndrome: a causally heterogeneous disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Congenital cardiovascular malformations: questions on inheritance. Baltimore-Washington Infant Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Identification of disease genes by whole genome CGH arrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Insights into the genetic basis of congenital heart disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31818095D0