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…
FDNA Inc. Launches New Face2Gene Suite of Phenotyping Apps to Aid in Identification and Evaluation of Rare and Ultra-rare Genetic Disorders
BUSINESS WIRE–“FDNA Inc. announced today at the American Society of Human Genetics (ASHG) Annual Meeting the launch of its new Face2Gene suite of phenotyping apps, facilitating comprehensive and precise genetic evaluations. Face2Gene increases confidence in clinical evaluations and improves the interpretation of genetic testing by filtering and prioritizing relevant variants.”
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Interview with Dr. Giulia Pascolini: Unravelling the Genetic Underpinnings of Dermatological Anomalies
Dr Giulia Pascolini, an esteemed Italian M.D. and Ph.D., is currently responsible for the Genetic Counselling Service of the Istituto…
Spanish Coffin Siris Syndrome Association: Fighting for Health and Recognition
Founded in 2017, the Spanish Coffin Siris Syndrome Association is an organization dedicated to supporting families affected by this rare…