Consanguinity mapping of congenital heart disease in a South Indian population (Q33565596)

28 July 2017

Consanguinity mapping of congenital heart disease in a South Indian population (English)

1 reference

28 July 2017

0 references

0 references

congenital heart disease

1 reference

Tracy L McGregor

1

1 reference

28 July 2017

Amit Misri

2

1 reference

28 July 2017

Jackie Bartlett

3

1 reference

28 July 2017

Guilherme Orabona

4

1 reference

28 July 2017

Richard D Friedman

5

1 reference

28 July 2017

David Sexton

6

1 reference

28 July 2017

Sunita Maheshwari

7

1 reference

28 July 2017

Thomas M Morgan

8

1 reference

28 July 2017

language of work or name

English

0 references

publication date

21 April 2010

1 reference

28 July 2017

1 reference

28 July 2017

5

1 reference

28 July 2017

4

1 reference

28 July 2017

e10286

1 reference

Creative Commons Attribution 4.0 International

28 July 2017

start time

21 April 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Targeted capture and massively parallel sequencing of 12 human exomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

The UCSC Genome Browser Database: update 2009

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Using population mixtures to optimize the utility of genomic databases: linkage disequilibrium and association study design in India

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

The Autism Genome Project: goals and strategies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Homez, a homeobox leucine zipper gene specific to the vertebrate lineage

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Defining the autism minimum candidate gene region on chromosome 7.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Finding genetic contributions to sporadic disease: a recessive locus at 12q24 commonly contributes to patent ductus arteriosus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

The incidence of congenital heart disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

An autosomal genomic screen for autism. Collaborative linkage study of autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Congenital heart disease in India: a status report.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Prevalence of congenital heart disease

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Parental consanguinity and congenital heart malformations in a developing country.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Contribution of birth defects to infant mortality in the United States

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

An autosomal genomic screen for autism.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Incorporating language phenotypes strengthens evidence of linkage to autism.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2858208

Pharmacokinetics and safety of intravenously administered citrulline in children undergoing congenital heart surgery: Potential therapy for postoperative pulmonary hypertension

31 October 2018

1 reference

12 December 2020

Individual genomes on the horizon

1 reference

12 December 2020

Properties of the transmission-disequilibrium test in the presence of inbreeding

1 reference

12 December 2020

Consanguinity and congenital heart disease in Saudi Arabia

1 reference

12 December 2020

First-cousin matings and congenital heart disease in Saudi Arabia

1 reference

12 December 2020

Parental consanguinity increases congenital heart diseases in South India

1 reference

12 December 2020

Congenital heart disease and parental consanguinity in South India

1 reference

12 December 2020

Nitric oxide precursors and congenital heart surgery: A randomized controlled trial of oral citrulline

1 reference

12 December 2020

A new gene, EVC2, is mutated in Ellis-van Creveld syndrome

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0010286

Identifiers

DOI

1 reference

28 July 2017

0 references

1 reference

28 July 2017

1 reference