| scholarly article | Q13442814 |
| P50 | author | Herbert Pratt | Q56445642 |
| Richard Francis | Q62915358 | ||
| Kimimasa Tobita | Q77812515 | ||
| P2093 | author name string | Cecilia W Lo | |
| Linda Leatherbury | |||
| Xiaoqin Liu | |||
| William Devine | |||
| Laura Reinholdt | |||
| Guozhen Chen | |||
| Ricardo Ramirez | |||
| Andrew J Kim | |||
| Judy Morgan | |||
| Liyin Wong | |||
| Ramiah Subramanian | |||
| Shane Anderton | |||
| Youngsil Kim | |||
| P2860 | cites work | The Hand1 and Hand2 transcription factors regulate expansion of the embryonic cardiac ventricles in a gene dosage-dependent manner | Q28505600 |
| The incidence of congenital heart disease | Q29614195 | ||
| Outflow tract cushions perform a critical valve-like function in the early embryonic heart requiring BMPRIA-mediated signaling in cardiac neural crest | Q30478829 | ||
| Genome-wide identification of mouse congenital heart disease loci | Q34013514 | ||
| Capitalizing on large-scale mouse mutagenesis screens | Q34186639 | ||
| ENU mutagenesis: analyzing gene function in mice | Q34433507 | ||
| Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve | Q34965424 | ||
| Cardiovascular defects in a mouse model of HOXA1 syndrome | Q35605185 | ||
| Rapid high resolution three dimensional reconstruction of embryos with episcopic fluorescence image capture | Q35923484 | ||
| Genetics of human heterotaxias | Q36298333 | ||
| Microcomputed tomography provides high accuracy congenital heart disease diagnosis in neonatal and fetal mice. | Q37537336 | ||
| Imaging modalities to assess structural birth defects in mutant mouse models | Q37791094 | ||
| Incidence of congenital heart disease: II. Prenatal incidence | Q40417373 | ||
| ENU induced mutations causing congenital cardiovascular anomalies | Q45153465 | ||
| Cardiovascular phenotyping of fetal mice by noninvasive high-frequency ultrasound facilitates recovery of ENU-induced mutations causing congenital cardiac and extracardiac defects | Q46713408 | ||
| Noninvasive localization of nuclear factor of activated T cells c1-/- mouse embryos by ultrasound biomicroscopy-Doppler allows genotype-phenotype correlation. | Q51957453 | ||
| Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1 | Q58193297 | ||
| Equivalent ages in mouse and human embryos | Q73641690 | ||
| Prenatal sonographic diagnosis of congenital heart disease and intrauterine growth restriction: a case-control study | Q80510234 | ||
| Prenatal ultrasound screening of congenital heart disease in an unselected national population: a 21-year experience | Q82919496 | ||
| Epidemiology of Ebstein anomaly: prevalence and patterns in Texas, 1999-2005 | Q83782728 | ||
| Cardiac malformations in spontaneous abortions | Q93632892 | ||
| P433 | issue | 1 | |
| P921 | main subject | echocardiography | Q216933 |
| congenital disorder | Q727096 | ||
| P304 | page(s) | 31-42 | |
| P577 | publication date | 2013-12-06 | |
| P1433 | published in | Circulation: Cardiovascular Imaging | Q3332375 |
| P1476 | title | Interrogating congenital heart defects with noninvasive fetal echocardiography in a mouse forward genetic screen | |
| P478 | volume | 7 |
| Q35180480 | ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning |
| Q26799556 | Bioengineering and Stem Cell Technology in the Treatment of Congenital Heart Disease |
| Q24303570 | CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation |
| Q26849750 | Capturing structure and function in an embryonic heart with biophotonic tools. |
| Q27334689 | Cardiac Light-Sheet Fluorescent Microscopy for Multi-Scale and Rapid Imaging of Architecture and Function |
| Q30362134 | Cardiovascular Imaging in Mice |
| Q50457524 | Cilia and Ciliopathies in Congenital Heart Disease |
| Q48124644 | Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families |
| Q91793465 | Evolution of care pathways for babies with hypoplastic left heart syndrome: integrating mechanistic and clinical process investigation, standardization, and collaborative study |
| Q27316952 | Global genetic analysis in mice unveils central role for cilia in congenital heart disease |
| Q36173712 | Hypoplastic left heart syndrome is associated with structural and vascular placental abnormalities and leptin dysregulation |
| Q44622965 | Micro-CT imaging: Developing criteria for examining fetal skeletons in regulatory developmental toxicology studies - A workshop report |
| Q96431887 | Mutation of LRP1 in cardiac neural crest cells causes congenital heart defects by perturbing outflow lengthening |
| Q24336897 | Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies |
| Q55072686 | Phenotyping cardiac and structural birth defects in fetal and newborn mice. |
| Q36736933 | Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects. |
| Q52430968 | The Genetic Landscape of Hypoplastic Left Heart Syndrome. |
| Q36377531 | The complex genetics of hypoplastic left heart syndrome. |
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