A Novel Case of Biliary Atresia in a Premature Neonate With 1p36 Deletion Syndrome
Author:
Affiliation:
1. University of Nevada, Las Vegas, NV, USA
2. Sunrise Children’s Hospital, Las Vegas, NV, USA
3. University Medical Center, Las Vegas, NV, USA
Publisher
SAGE Publications
Subject
Safety Research,Safety, Risk, Reliability and Quality,Epidemiology
Link
http://journals.sagepub.com/doi/pdf/10.1177/2324709618790613
Reference11 articles.
1. Terminal deletion of 1p36
2. 1p36 deletion syndrome with intestinal malrotation and annular pancreas
3. A Case of 1p36 Deletion Syndrome Accompanied With Anomalous Arrangement of the Pancreaticobiliary Duct
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1. Genetic Contributions to Biliary Atresia: A Developmental Cholangiopathy;Seminars in Liver Disease;2023-08
2. Prenatal diagnosis of pure 1p36 terminal deletion by chromosome microarry analysis — clinical report of 3 new cases and review of the literature;Ginekologia Polska;2021-10-14
3. Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report;BMC Pediatrics;2020-05-09
4. Genetics in biliary atresia;Current Opinion in Gastroenterology;2019-03
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