Expanding the genetic landscape of <i>SLC4A1</i>-linked hereditary spherocytosis: discovery of a novel TM9 variant using high-resolution genomic profiling analysis. [PDF]
Front GenetMore TA, Kedar PS.
europepmc +1 more source
Hereditary hyperbilirubinemia: An original study of four cases with review of literature
IOSR Journal of Dental and Medical Sciences, 2014 Dr. Aarti B.Bhattacharya +2 more
openaire +1 more source
Recurrent Cholestatic Jaundice in a Young Indian Adult: A Clinical Diagnosis of Benign Recurrent Intrahepatic Cholestasis. [PDF]
CureusPanda SS +3 more
europepmc +1 more source
Presumptive Bilirubin-Related Chlorodontia and Developmental Enamel Defects of the Primary Dentition in an Extremely Preterm Infant: A Case Report. [PDF]
J Clin MedSzymczak-Paluch M +2 more
europepmc +1 more source
Genetic insights into unexplained infant jaundice: a study from northern Guangdong, China. [PDF]
Front PediatrGao F +5 more
europepmc +1 more source
Risk Assessment for Drug-Induced Hyperbilirubinemia: A Mechanistic Approach. [PDF]
CPT Pharmacometrics Syst PharmacolKumar R +4 more
europepmc +1 more source
Neonatal Conjugated Hyperbilirubinemia: Clinical Profile, Etiology, and Predictors of Adverse Outcomes in a NICU of a Tertiary Care Center. [PDF]
CureusRamya K +6 more
europepmc +1 more source
Case Report: Late-onset liver cirrhosis in an elderly patient with FBN1-related Geleophysic Dysplasia. [PDF]
Front Endocrinol (Lausanne)Liu Y, Wang Y, Teng X, Wang X.
europepmc +1 more source
A novel <i>ANK1</i> frameshift mutation associated with neonatal hereditary spherocytosis: a case report. [PDF]
Front PediatrQing X +5 more
europepmc +1 more source