Pages that link to "Q74045367"

The following pages link to Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects (Q74045367):

Displaying 23 items.

• 8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families (Q21202042) (← links)
• Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia (Q24650395) (← links)
• Identification of candidate genes for congenital heart defects on proximal chromosome 8p. (Q30827321) (← links)
• Periconceptional nutrient intakes and risks of conotruncal heart defects (Q33770519) (← links)
• From microscopes to microarrays: dissecting recurrent chromosomal rearrangements (Q33805828) (← links)
• Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements (Q33936335) (← links)
• Genetic basis of congenital cardiovascular malformations (Q34125381) (← links)
• Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level (Q34439909) (← links)
• A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects (Q34979568) (← links)
• Genetic Variants in Isolated Ebstein Anomaly Implicated in Myocardial Development Pathways. (Q36176207) (← links)
• Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qter (Q37113395) (← links)
• GATA4 sequence variants in patients with congenital heart disease (Q37120985) (← links)
• Transcription factor pathways and congenital heart disease. (Q37997218) (← links)
• The general anesthesia experience of deletion 8p syndrome patient -A case report-. (Q39214524) (← links)
• Inverted duplications: how many of them are mosaic? (Q40533026) (← links)
• Isolated chromosome 8p23.2‑pter deletion: Novel evidence for developmental delay, intellectual disability, microcephaly and neurobehavioral disorders (Q41918413) (← links)
• De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome. (Q52680610) (← links)
• Pre- and Postnatal Diagnosis of 5q35.1 and 8p23.1 Deletion in Congenital Heart Disease. (Q53155317) (← links)
• [Pediatric cardiology in the genomic era]. (Q53640842) (← links)
• Increased prevalence of cardiovascular defects among 56,709 California twin pairs. (Q55155251) (← links)
• Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect (Q64044400) (← links)
• Is interstitial 8p23 microdeletion responsible of 46,XY gonadal dysgenesis? One case report from birth to puberty (Q64265009) (← links)
• Inherited duplication, dup (8) (p23.1p23.1) pat, in a father and daughter with congenital heart defects (Q77359238) (← links)