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12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes.
Risk of coronary artery injury with radiofrequency ablation and cryoablation of epicardial posteroseptal accessory pathways within the coronary venous system.
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12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes.
12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes. Clin Dysmorphol. 2012 Apr; 21(2):93-96.
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PubMed
subject areas
Cadherins
Child
Chromosome Deletion
Chromosome Disorders
Chromosomes, Human, Pair 4
Facies
Factor XI
Humans
Male
Receptor, Melatonin, MT1