Genetic disorders among Arab populations

od Teebi, Ahmad S.
Izdano 2010

Phenotypic Heterogeneity in Woodhouse-Sakati Syndrome: Two New Families with a Mutation in the C2orf37 Gene

od Ben-Omran, Tawfeg, Ali, Rehab, Almureikhi, Mariam, Alameer, Seham, Al-Saffar, Muna, Walsh, Christopher A., Felie, Jillian M., Teebi, Ahmad
Izdano u Am J Med Genet A (2011)

Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta Syndrome

od Anastasio, Natascia, Ben-Omran, Tawfeg, Teebi, Ahmad, Ha, Kevin C.H., Lalonde, Emilie, Ali, Rehab, Almureikhi, Mariam, Der Kaloustian, Vazken M., Liu, Junhui, Rosenblatt, David S., Majewski, Jacek, Jerome-Majewska, Loydie A.
Izdano 2010

Mutations in Capillary Morphogenesis Gene-2 Result in the Allelic Disorders Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis

od Dowling, Oonagh, Difeo, Analisa, Ramirez, Maria C., Tukel, Turgut, Narla, Goutham, Bonafe, Luisa, Kayserili, Hulya, Yuksel-Apak, Memnune, Paller, Amy S., Norton, Karen, Teebi, Ahmad S., Grum-Tokars, Valerie, Martin, Gail S., Davis, George E., Glucksman, Marc J., Martignetti, John A.
Izdano 2003

Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects

od Wouters, Vinciane, Limaye, Nisha, Uebelhoer, Melanie, Irrthum, Alexandre, Boon, Laurence M, Mulliken, John B, Enjolras, Odile, Baselga, Eulalia, Berg, Jonathan, Dompmartin, Anne, Ivarsson, Sten A, Kangesu, Loshan, Lacassie, Yves, Murphy, Jill, Teebi, Ahmad S, Penington, Anthony, Rieu, Paul, Vikkula, Miikka
Izdano 2010

Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes

od Kantarci, Sibel, Al-Gazali, Lihadh, Hill, R Sean, Donnai, Dian, Black, Graeme C M, Bieth, Eric, Chassaing, Nicolas, Lacombe, Didier, Devriendt, Koen, Teebi, Ahmad, Loscertales, Maria, Robson, Caroline, Liu, Tianming, MacLaughlin, David T, Noonan, Kristin M, Russell, Meaghan K, Walsh, Christopher A, Donahoe, Patricia K, Pober, Barbara R
Izdano 2007

Additional EFNB1 Mutations in Craniofrontonasal Syndrome

od Wallis, Deeann, Lacbawan, Felicitas, Jain, Mahim, Der Kaloustian, Vazken M., Steiner, Carlos E., Moeschler, John B., Losken, H. Wolfgang, Kaitila, Ilkka I., Cantrell, Stephen, Proud, Virginia K., Carey, John C., Day, Donald W., Lev, Dorit, Teebi, Ahmad S., Robinson, Luther K., Hoyme, H. Eugene, Al-Torki, Nadia, Siegel-Bartelt, Jacqueline, Mulliken, John B., Robin, Nathaniel H., Saavedra, Dolores, Zackai, Elaine H., Muenke, Maximilian
Izdano 2008

Structural Variation of Chromosomes in Autism Spectrum Disorder

od Marshall, Christian R., Noor, Abdul, Vincent, John B., Lionel, Anath C., Feuk, Lars, Skaug, Jennifer, Shago, Mary, Moessner, Rainald, Pinto, Dalila, Ren, Yan, Thiruvahindrapduram, Bhooma, Fiebig, Andreas, Schreiber, Stefan, Friedman, Jan, Ketelaars, Cees E.J., Vos, Yvonne J., Ficicioglu, Can, Kirkpatrick, Susan, Nicolson, Rob, Sloman, Leon, Summers, Anne, Gibbons, Clare A., Teebi, Ahmad, Chitayat, David, Weksberg, Rosanna, Thompson, Ann, Vardy, Cathy, Crosbie, Vicki, Luscombe, Sandra, Baatjes, Rebecca, Zwaigenbaum, Lonnie, Roberts, Wendy, Fernandez, Bridget, Szatmari, Peter, Scherer, Stephen W.
Izdano 2008