Show 5 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="Bozorgmehr, Bita" or (type exact bookEditor and editor="Bozorgmehr, Bita") Add to list Journal Article A1 open access Discriminative features in three autosomal recessive cutis laxa syndromes : cutis laxa IIA, cutis laxa IIB, and geroderma osteoplastica Ariana Kariminejad, Fariba Afroozan, Bita Bozorgmehr, Alireza Ghanadan, Susan Akbaroghli, Hamid Reza Khorram Khorshid, Faezeh Mojahedi, Aria Setoodeh, Abigail Loh, Yu Xuan Tan, et al. (2017) INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 18(3). Add to list Journal Article A1 Retinitis pigmentosa, cutis laxa and pseudoxanthoma elasticum-like skin manifestations associated with GGCX mutations Ariana Kariminejad, Bita Bozorgmehr, Abdolhamid Najafi, Atefeh Khoshaeen, Maryam Ghalandari, Hossein Najmabadi, Mohamad Hasan Kariminejad, Olivier Vanakker (UGent) , Mohammad Jakir Hosen (UGent) , Fransiska Malfait (UGent) , et al. (2014) JOURNAL OF INVESTIGATIVE DERMATOLOGY. 134(9). p.2331-2338 Add to list Journal Article A1 Defective initiation of glycosaminoglycan synthesis due to B3GALT6 mutations causes a pleiotropic Ehlers-Danlos-syndrome-like connective tissue disorder Fransiska Malfait (UGent) , Ariana Kariminejad, Tim Van Damme (UGent) , Caroline Gauche, Delfien Syx (UGent) , Faten Merhi-Soussi, Sandrine Gulberti, Sofie Symoens (UGent) , Suzanne Vanhauwaert (UGent) , Andy Willaert (UGent) , et al. (2013) AMERICAN JOURNAL OF HUMAN GENETICS. 92(6). p.935-945