Pages that link to "Q73670410"
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The following pages link to A Genetic Etiology for Interruption of the Aortic Arch Type B (Q73670410):
Displaying 31 items.
- Epigenetic mechanisms in cardiac development and disease (Q26853290) (← links)
- Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice (Q28586874) (← links)
- Isolated interrupted aortic arch: unexpected diagnosis in a 63-year-old male (Q33566031) (← links)
- Chromosomal abnormalities among children born with conotruncal cardiac defects (Q33797160) (← links)
- Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease (Q34214613) (← links)
- Multislice CT angiography of interrupted aortic arch. (Q36983777) (← links)
- 22q11.2 deletion syndrome (Q36988231) (← links)
- 22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development (Q37669766) (← links)
- The three-vessel view in the fetal mediastinum in the diagnosis of interrupted aortic arch (Q37917238) (← links)
- Congenital Thoracic Vascular Anomalies: Evaluation with State-of-the-Art MR Imaging and MDCT (Q37925924) (← links)
- Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome) (Q39654228) (← links)
- Atresia of the aortic arch, with a collateral artery from the right subclavian artery supplying the descending aorta (Q46841391) (← links)
- The Jing-Mai connections of the Heart (Q47397348) (← links)
- Interrupted aortic arch complicated with takotsubo cardiomyopathy mimicking aortic dissection. (Q48026936) (← links)
- Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome (Q50420674) (← links)
- The aberrant right subclavian artery (arteria lusoria): the morphological and clinical aspects of one of the most important variations--a systematic study of 141 reports. (Q51122064) (← links)
- Developmental anomalies of the outflow tracts and aortic arch: towards an understanding of the role of deletions within the 22nd chromosome. (Q52173575) (← links)
- Congenital heart defects and 22q11 deletions: which genes count? (Q52184039) (← links)
- Deletion 22q11 in patients with interrupted aortic arch (Q58193949) (← links)
- Loss of CXCL12/CXCR4 signalling impacts several aspects of cardiovascular development but does not exacerbate Tbx1 haploinsufficiency (Q58588198) (← links)
- Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice (Q64096984) (← links)
- Failed Progenitor Specification Underlies the Cardiopharyngeal Phenotypes in a Zebrafish Model of 22q11.2 Deletion Syndrome. (Q64884964) (← links)
- Interruption of the aortic arch associated with deletion of chromosome 22q11 is associated with a subarterial and doubly committed ventricular septal defect in Japanese patients (Q73118269) (← links)
- Interruption of the aortic arch at the isthmus with DiGeorge syndrome and 22q11.2 deletion (Q73118303) (← links)
- Anatomic patterns of conotruncal defects associated with deletion 22q11 (Q73840767) (← links)
- Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching (Q74070188) (← links)
- Cervical origin of the subclavian artery as a specific marker for monosomy 22q11 (Q77616520) (← links)
- Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes? (Q80428079) (← links)
- Complete aortic arch obstruction: interruption or aortic coarctation? (Q81518711) (← links)
- 22q11.2 deletion syndrome and complex congenital heart defects (Q83577008) (← links)
- Pax9 is required for cardiovascular development and interacts with Tbx1 in the pharyngeal endoderm to control 4th pharyngeal arch artery morphogenesis (Q92831284) (← links)