Implications of genetic testing in noncompaction/hypertrabeculation
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.c.31371/fullpdf
Reference52 articles.
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3. Further delineation of deletion 1p36 syndrome in 60 patients: A recognizable phenotype and common cause of developmental delay and mental retardation;Battaglia;Pediatrics,2008
4. A neonatal case of left ventricular noncompaction associated with trisomy 18;Beken;Genet Couns,2011
5. Standardized human pedigree nomenclature: Update and assessment of the recommendations of the National Society of Genetic Counselors;Bennett;J Genet Couns,2008
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2. Emerging Hallmarks of Mitochondrial Biochemistry in Cardiac Trabecular Morphogenesis and Left Ventricular Noncompaction (LVNC);New Insights on Cardiomyopathy [Working Title];2022-12-20
3. Genetic Testing in Pediatric Left Ventricular Noncompaction;Circulation: Cardiovascular Genetics;2017-12
4. Left ventricular noncompaction cardiomyopathy in a patient with trisomy 13: A report and review of the literature;American Journal of Medical Genetics Part A;2017-05-09
5. Pathophysiology of Cardiomyopathies;Fetal and Neonatal Physiology;2017
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