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J David Brook

Showing results (41-50 of 45) with videos related to

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Circulation. Cardiovascular Genetics|July 24, 2013
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controlsChrysovalanto Mamasoula, R Reid Prentice, Tomasz Pierscionek, et al.
Plos Genetics|September 21, 2021
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Human Molecular Genetics|March 12, 2016
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20Neil A Hanchard, Shanker Swaminathan, Kristine Bucasas, et al.
Plos Genetics|July 29, 2021
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Nature Genetics|August 2, 2016
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencingAlejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, et al.
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Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Circulation. Cardiovascular Genetics|July 24, 2013
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controlsChrysovalanto Mamasoula, R Reid Prentice, Tomasz Pierscionek, et al.
Plos Genetics|September 21, 2021
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Human Molecular Genetics|March 12, 2016
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20Neil A Hanchard, Shanker Swaminathan, Kristine Bucasas, et al.
Plos Genetics|July 29, 2021
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Nature Genetics|August 2, 2016
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencingAlejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, et al.
Pageof 5