Fetal Fentanyl Syndrome: Unveiling a New Syndrome Linked to Fentanyl Use During Pregnancy
Dr. Karen Gripp, MD, Chief of the Division of Medical Genetics at Nemours Children’s Health in Wilmington, has been at…
October 11, 2017
“Murdoch Children’s Research Institute (MCRI) and the Victorian Clinical Genetics Service (VCGS) have partnered with Boston-based FDNA for full integration and exclusive distribution of MCRI’s POSSUMweb database through FDNA’s Face2Gene suite of software applications. POSSUMweb’s database integration will assist clinicians in shortening the diagnostic timeline for patients by providing insights from over 4,000 syndromes, including multiple malformations, metabolic, teratogenic, chromosomal, and skeletal syndromes.”
Dr. Karen Gripp, MD, Chief of the Division of Medical Genetics at Nemours Children’s Health in Wilmington, has been at…
Dr Giulia Pascolini, an esteemed Italian M.D. and Ph.D., is currently responsible for the Genetic Counselling Service of the Istituto…
Founded in 2017, the Spanish Coffin Siris Syndrome Association is an organization dedicated to supporting families affected by this rare…