A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus

التفاصيل البيبلوغرافية
العنوان: A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus
المؤلفون: Livia Garavelli, L. Matalonga, Ivan Ivanovski, Stefano Giuseppe Caraffi, Ilenia Maini, Steven Laurie, Chiara Baldo, Chiara Gelmini, Simonetta Rosato, Marzia Pollazzon, M.L. De Bernardi, E. Farnetti
المصدر: Neuropediatrics. 49:222-224
بيانات النشر: Georg Thieme Verlag KG, 2018.
سنة النشر: 2018
مصطلحات موضوعية: 0301 basic medicine, Postaxial polydactyly, Pathology, medicine.medical_specialty, Fingers, 03 medical and health sciences, medicine, Cyclin D2, Humans, Megalencephaly, Child, business.industry, General Medicine, Toes, medicine.disease, Perisylvian polymicrogyria, Hydrocephalus, Polydactyly, 030104 developmental biology, Polymicrogyria, Mutation, Pediatrics, Perinatology and Child Health, Mutation (genetic algorithm), Female, Neurology (clinical), business
تدمد: 1439-1899
0174-304X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44486ec623267c2f63d109cf8bb1f342Test
https://doi.org/10.1055/s-0038-1641722Test
رقم الانضمام: edsair.doi.dedup.....44486ec623267c2f63d109cf8bb1f342
قاعدة البيانات: OpenAIRE