The 20 Best Chromosome 13q Duplication Doctors in Missouri, US

Renuka Peterson is a Pediatric Cardiologist in St. Louis, Missouri. Dr. Peterson is rated as a Distinguished provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Chromosome 13q Duplication, Trisomy 13, Pulmonary Atresia with Intact Ventricular Septum, and Pulmonary Atresia.

Nandini Calamur is a Palliative Medicine provider in Saint Louis, Missouri. Dr. Calamur is rated as a Distinguished provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Chromosome 13q Duplication and Trisomy 13.

Dr. Kimberly Spence provides care for premature and extremely premature infants, normal and sick newborns, babies in Level II-IV neonatal intensive care, and offers consultation services for expectant mothers. She also treats babies who receive outpatient care in the high-risk nursery clinic. Dr. Spence is involved in palliative care, with particular interest in ethical issues related to end-of-life care. She specializes in quality improvement initiatives and neonatal abstinence syndrome. Her research interests include the improvement of care to the families of infants with neonatal abstinence syndrome. Dr. Spence is an associate professor in the Department of Pediatrics, Division of Neonatology, at Saint Louis University School of Medicine. Dr. Spence is rated as a Distinguished provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Chromosome 13q Duplication, Trisomy 13, and Neonatal Abstinence Syndrome.

Dr. Stephen Braddock provides genetic evaluations, diagnoses, and counseling for patients of all ages. This includes services not exclusive to pediatric patients, but also prenatal counseling, cancer counseling, and adult genetic disorders. He specializes in delineation of new multiple malformation syndromes, dysmorphology, prevalence and variation of prenatal teratogen exposures and birth defects, and fetal alcohol syndrome. His research interests include teratology, fetal alcohol syndrome, and dysmorphology/syndrome delineation. Dr. Braddock is director of medical genetics and a professor in the Department of Pediatrics, Division of Medical Genetics, at Saint Louis University School of Medicine. He is a fellow of the American College of Medical Genetics and Genomics, and the American Academy of Pediatrics. He is a member of the American Society of Human Genetics, the Teratology Society, and the Organization of Teratogen Information Services. Dr. Braddock is a sports history/trivia buff, particularly baseball history. He owns two Babe Ruth baseball cards. Dr. Braddock is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Chromosome 20 Trisomy, Cerebellar Hypoplasia, CHARGE Syndrome, and Coloboma.

Dr. Justin Josephsen specializes in the care of critically ill newborns. He is interested in community outreach and in research regarding simulation-based medical education, as well as improving management of frail neonates in the delivery room. Dr. Josephsen is an assistant professor in the Department of Pediatrics, Division of Neonatology, at Saint Louis University School of Medicine. He is a member of the American Academy of Pediatrics and the American Pediatric Association. Dr. Josephsen is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Premature Infant, Intraventricular Hemorrhage of the Newborn, Chromosome 13q Duplication, and Trisomy 13.

Dr. Josh Arthur practices general pediatrics, with special interest in patient communication, parent education, health care ethics, and theology and medicine. He provides both inpatient and outpatient services. Dr. Arthur is an associate professor in the Department of Pediatrics, Division of General Academic Pediatrics, at Saint Louis University School of Medicine. His interests outside of work include singing and playing the guitar. Dr. Arthur is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Chromosome 13q Duplication, Trisomy 13, Delayed Growth, and Obesity.

Dr. Catherine Cibulskis is a newborn specialist whose patients include infants from sick full-term newborns to extremely premature infants. She provides Level II-IV neonatal intensive care and attends high-risk deliveries. Dr. Cibulskis also offers antenatal consultation for expectant mothers, as well as outpatient care in the high-risk nursery follow-up clinic. Dr. Cibulskis pursues a variety of research interests. She is involved in improving neonatal nutrition for vulnerable infants. She is also involved in several studies in association with the St. Louis Fetal Care Institute, looking at prenatal factors and outcomes in congenital anomalies and complicated pregnancies. Dr. Cibulskis is an associate professor in the Department of Pediatrics, Division of Neonatal-Perinatal Medicine, at Saint Louis University School of Medicine. She has authored numerous medical abstracts and publications, and is a frequent lecturer on improving the care of NICU patients. She is a fellow of the American Academy of Pediatrics. Dr. Cibulskis is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Myelomeningocele, Necrotizing Enterocolitis, Chromosome 13q Duplication, and Trisomy 13.