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| Deep Phenotyping in 1p36 Deletion Syndrome |
| Youngkyu Shim, Young Jun Go, Soo Yeon Kim, Hunmin Kim, Hee Hwang, Jieun Choi, Byung Chan Lim, Ki Joong Kim, Jong-Hee Chae |
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Ann Child Neurol. 2020;28(4):131-137. Published online August 13, 2020 DOI: https://doi.org/10.26815/acn.2020.00108 |
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Deep Phenotyping in 1p36 Deletion Syndrome Annals of Child Neurology. 2020;28(4):131-137  Growth patterns of patients with 1p36 deletion syndrome Congenital Anomalies. 2014;54(2):82-86 1p36 deletion syndrome associated with Prader-Willi-like phenotype Pediatrics International. 2010;52(4):547-550 1p36 deletion syndrome: an update The Application of Clinical Genetics. 2015;189 DELETION 1p36 SYNDROME Cassidy and Allanson's Management of Genetic Syndromes. 2020;253-264 Follicular Bronchiolitis in a Child With 1p36 Deletion Syndrome Chest. 2015;148(4):631A Dying at 23 with 1p36 deletion syndrome: Laura's family story Internal Medicine Journal. 2012;42(9):1037-1039 Multiple causes of apnea in 1p36 deletion syndrome include seizures Seizure. 2012;21(5):402-406 Psychiatric Comorbidities in 1p36 Deletion Syndrome and Their Treatment—A Case Report International Journal of Environmental Research and Public Health. 2021;18(22):12064 Pathologic Features of Dilated Cardiomyopathy with Localized Noncompaction in a Child with Deletion 1p36 Syndrome Congenital Heart Disease. 2011;7(1):59-61 |
