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American Journal of Human Genetics|August 20, 2004
NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlationsLynette A Gillis, Jennifer McCallum, Maninder Kaur, et al.Journal of the American College of Surgeons|April 10, 2020
Population-Based Analysis of Hepatocellular Carcinoma in Children: Identifying Optimal Surgical TreatmentIoannis A Ziogas, Fei Ye, Zhiguo Zhao, et al.The American Journal of Surgical Pathology|June 22, 2024
Clinical and Histopathologic Characteristics of Acute Severe Hepatitis Associated With Human Herpesvirus 6 InfectionHuiying Wang, Annette Vannilam, Einar T Hafberg, et al.Hepatology (Baltimore, Md.)|August 3, 2018
Safety and Efficacy of Ledipasvir-Sofosbuvir With or Without Ribavirin for Chronic Hepatitis C in Children Ages 6-11Karen F Murray, William F Balistreri, Sanjay Bansal, et al.Nature Genetics|May 18, 2004
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-BIan D Krantz, Jennifer McCallum, Cheryl DeScipio, et al.Hepatology (Baltimore, Md.)|June 22, 2019
Sofosbuvir and Ribavirin Therapy for Children Aged 3 to <12 Years With Hepatitis C Virus Genotype 2 or 3 InfectionPhilip Rosenthal, Kathleen B Schwarz, Regino P Gonzalez-Peralta, et al.Journal of Pediatric Gastroenterology and Nutrition|January 15, 2019
Clinical Practice Approach to Nonalcoholic Fatty Liver Disease by Pediatric Gastroenterologists in the United StatesWarren L Shapiro, Elizabeth L Yu, Jennifer C Arin, et al.Human Mutation|March 7, 2014
Mutations in the human UBR1 gene and the associated phenotypic spectrumMaja Sukalo, Ariane Fiedler, Celina Guzmán, et al.Pageof 2