A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy

por Farajzadeh Valilou, Saeed, Karimzad Hagh, Javad, Salimi Asl, Mohammad, Abdi Rad, Isa, Edizadeh, Masoud, Pooladi, Arash
Publicado 2021

Characterization of a Rare Mosaicism in Autosomal Translocation of t(5;21) Using Conventional Cytogenetics and FISH Methods

por Omori Sarabi, Sadaf, Karimzad Hagh, Javad, Behrend, Claudia, Mohseni, Seyed Behrooz, Ansari Dezfouli, Mitra, Rashidi, Seyed Khalil, Omrani, Mir Davood
Publicado 2020

Prenatal Diagnosis of Mosaic Tetrasomy 18p in a Case without Sonographic Abnormalities

por Karimzad Hagh, Javad, Liehr, Thomas, Ghaedi, Hamid, Mossalaeie, Mir Majid, Alimohammadi, Shohreh, Inanloo Hajiloo, Faegheh, Moeini, Zahra, Sarabi, Sadaf, Zare-Abdollahi, Davood
Publicado 2017