CrossRef Text and Data Mining
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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
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   Crossref logo
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Growth patterns of patients with 1p36 deletion syndrome
Congenital Anomalies. 2014;54(2):82-86   Crossref logo
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1p36 deletion syndrome associated with Prader-Willi-like phenotype
Pediatrics International. 2010;52(4):547-550   Crossref logo
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1p36 deletion syndrome: an update
The Application of Clinical Genetics. 2015;189   Crossref logo
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DELETION 1p36 SYNDROME
Cassidy and Allanson's Management of Genetic Syndromes. 2020;253-264   Crossref logo
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Follicular Bronchiolitis in a Child With 1p36 Deletion Syndrome
Chest. 2015;148(4):631A   Crossref logo
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Dying at 23 with 1p36 deletion syndrome: Laura's family story
Internal Medicine Journal. 2012;42(9):1037-1039   Crossref logo
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Multiple causes of apnea in 1p36 deletion syndrome include seizures
Seizure. 2012;21(5):402-406   Crossref logo
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Psychiatric Comorbidities in 1p36 Deletion Syndrome and Their Treatment—A Case Report
International Journal of Environmental Research and Public Health. 2021;18(22):12064   Crossref logo
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Pathologic Features of Dilated Cardiomyopathy with Localized Noncompaction in a Child with Deletion 1p36 Syndrome
Congenital Heart Disease. 2011;7(1):59-61   Crossref logo
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