Biliary atresia combined with progressive familial intrahepatic cholestasis type 3
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference38 articles.
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1. A novel heterozygous deletion in ABCB4 gene in a Chinese family with intrahepatic cholestasis of pregnancy, neonatal hyperbilirubinemia, and cholelithiasis: Case reports and literature review;Molecular Genetics & Genomic Medicine;2023-10-03
2. Type 3 of progressive familial intrahepatic cholestasis (PFIC‐3): Case report;Clinical Case Reports;2023-04
3. Biliary atresia and its mimics;Diagnostic Histopathology;2023-01
4. Aetiology and outcomes of prolonged neonatal jaundice in tertiary centres: data from the China Neonatal Genome Project;Archives of Disease in Childhood - Fetal and Neonatal Edition;2022-07-18
5. PHENOTYPIC AND GENOTYPIC CHARACTERISTICS OF PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS TYPE 3 IN PEDIATRIC POPULATION IN PAKISTAN;KHYBER MEDICAL UNIVERSITY JOURNAL;2022-03-31
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