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Judith A Goodship

Showing results (51-60 of 57) with videos related to

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Human Molecular Genetics|January 9, 2013
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of FallotHeather J Cordell, Ana Töpf, Chrysovalanto Mamasoula, et al.
American Journal of Human Genetics|August 4, 2015
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter DevelopmentAsaf Vivante, Marc-Jens Kleppa, Julian Schulz, et al.
Nature Genetics|May 28, 2013
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16Heather J Cordell, Jamie Bentham, Ana Topf, et al.
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.
Journal of the American Society of Nephrology : JASN|August 23, 2014
Urinary tract effects of HPSE2 mutationsHelen M Stuart, Neil A Roberts, Emma N Hilton, et al.
Nature Communications|May 26, 2017
Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valveBo Yang, Wei Zhou, Jiao Jiao, 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.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Human Molecular Genetics|January 9, 2013
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of FallotHeather J Cordell, Ana Töpf, Chrysovalanto Mamasoula, et al.
American Journal of Human Genetics|August 4, 2015
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter DevelopmentAsaf Vivante, Marc-Jens Kleppa, Julian Schulz, et al.
Nature Genetics|May 28, 2013
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16Heather J Cordell, Jamie Bentham, Ana Topf, et al.
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.
Journal of the American Society of Nephrology : JASN|August 23, 2014
Urinary tract effects of HPSE2 mutationsHelen M Stuart, Neil A Roberts, Emma N Hilton, et al.
Nature Communications|May 26, 2017
Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valveBo Yang, Wei Zhou, Jiao Jiao, 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.
Pageof 6