Biotin-Responsive Basal Ganglia Disease Maps to 2q36.3 and Is Due to Mutations in SLC19A3

Por Zeng, Wen-Qi , Al-Yamani, Eiman , Acierno, Jr., James S. , Slaugenhaupt, Susan , Gillis, Tammy , MacDonald, Marcy E. , Ozand, Pinar T. , Gusella, James F. 
Publicado em 2005

Integrative and comparative genomics analysis of early hepatocellular carcinoma differentiated from liver regeneration in young and old

Por Colak, Dilek, Chishti, Muhammad A, Al-Bakheet, Al-Bandary, Al-Qahtani, Ahmed, Shoukri, Mohamed M, Goyns, Malcolm H, Ozand, Pinar T, Quackenbush, John, Park, Ben H, Kaya, Namik
Publicado em 2010

Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects

Por Sakati Nadia, Al-Odaib Ali, Al-Habit Ola, Colak Dilek, Alshidi Tarfa A, AbuDheim Nada, Al-Dosari Naji, Al-Zahrani Jawaher, Meyer Brian, Ozand Pinar T, Kaya Namik
Publicado em 2011-04-01

Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects

Por Al-Zahrani, Jawaher, Al-Dosari, Naji, AbuDheim, Nada, Alshidi, Tarfa A, Colak, Dilek, Al-Habit, Ola, Al-Odaib, Ali, Sakati, Nadia, Meyer, Brian, Ozand, Pinar T, Kaya, Namik
Publicado em 2011