المؤلفون: Pîrlog LM; Department of Molecular Sciences, Faculty of Medicine, University of Medicine and Pharmacy 'Iuliu Hațieganu', 400012 Cluj-Napoca, Romania., Pătrășcanu AA; Department of Molecular Sciences, Faculty of Medicine, University of Medicine and Pharmacy 'Iuliu Hațieganu', 400012 Cluj-Napoca, Romania., Militaru MS; Department of Molecular Sciences, Faculty of Medicine, University of Medicine and Pharmacy 'Iuliu Hațieganu', 400012 Cluj-Napoca, Romania.; Regional Laboratory Cluj-Napoca, Department of Medical Genetics, Regina Maria Health Network, 400363 Cluj-Napoca, Romania., Cătană A; Department of Molecular Sciences, Faculty of Medicine, University of Medicine and Pharmacy 'Iuliu Hațieganu', 400012 Cluj-Napoca, Romania.; Regional Laboratory Cluj-Napoca, Department of Medical Genetics, Regina Maria Health Network, 400363 Cluj-Napoca, Romania.; Department of Oncogenetics, 'Prof. Dr. I. Chiricuță' Institute of Oncology, 400015 Cluj-Napoca, Romania.

المصدر: Medicina (Kaunas, Lithuania) [Medicina (Kaunas)] 2024 May 06; Vol. 60 (5). Date of Electronic Publication: 2024 May 06.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 9425208 Publication Model: Electronic Cited Medium: Internet ISSN: 1648-9144 (Electronic) Linking ISSN: 1010660X NLM ISO Abbreviation: Medicina (Kaunas) Subsets: MEDLINE

مواضيع طبية MeSH: Hamartoma Syndrome, Multiple*/genetics , Hamartoma Syndrome, Multiple*/diagnosis , PTEN Phosphohydrolase*/genetics, Female ; Humans ; Proteus Syndrome/genetics ; Proteus Syndrome/diagnosis ; Male