Zobrazeno 1 - 10
of 1 798
pro vyhledávání: '"Alkuraya, Fowzan S"'
Autor:
Muggenthaler, Martina M. A., Chowdhury, Biswajit, Hasan, S. Naimul, Cross, Harold E., Mark, Brian, Harlalka, Gaurav V., Patton, Michael A., Ishida, Miho, Behr, Elijah R., Sharma, Sanjay, Zahka, Kenneth, Faqeih, Eissa, Blakley, Brian, Jackson, Mike, Lees, Melissa, Dolinsky, Vernon, Cross, Leroy, Stanier, Philip, Salter, Claire, Baple, Emma L., Alkuraya, Fowzan S., Crosby, Andrew H., Triggs-Raine, Barbara, Chioza, Barry A.
Orofacial clefting is amongst the most common of birth defects, with both genetic and environmental components. Although numerous studies have been undertaken to investigate the complexities of the genetic etiology of this heterogeneous condition, th
Externí odkaz:
http://hdl.handle.net/10150/623116
http://arizona.openrepository.com/arizona/handle/10150/623116
http://arizona.openrepository.com/arizona/handle/10150/623116
Autor:
De Hayr, Lachlan 1, 2, Blok, Laura E.R. 3, Dias, Kerith-Rae 4, 5, Long, Jingyi 3, Begemann, Anaïs 6, Moir, Robyn D. 7, Willis, Ian M. 7, Mocera, Martina 6, Siegel, Gabriele 6, Steindl, Katharina 6, Evans, Carey-Anne 4, 8, Zhu, Ying 8, Zhang, Futao 8, Field, Michael 9, Ma, Alan 10, 11, Adès, Lesley 10, 11, Josephi-Taylor, Sarah 10, 11, Pfundt, Rolph 3, Zaki, Maha S. 12, Tomoum, Hoda 13, Gregor, Anne 14, 15, Laube, Julia 6, Reis, André 15, Maddirevula, Sateesh 16, Hashem, Mais O. 16, Zweier, Markus 6, Alkuraya, Fowzan S. 16, 17, Maroofian, Reza 18, Buckley, Michael F. 8, Gleeson, Joseph G. 19, 20, Zweier, Christiane 14, 15, Coll-Tané, Mireia 3, Koolen, David A. 3, Rauch, Anita 6, 21, 22, Roscioli, Tony 4, 5, 8, Schenck, Annette 3, Harvey, Robert J. 1, 2, ∗
Publikováno v:
In Genetics in Medicine January 2025 27(1)
Autor:
Calame, Daniel G. 1, 2, 3, ∗, Wong, Jovi Huixin 4, Panda, Puravi 4, Nguyen, Dat Tuan 4, Leong, Nancy C.P. 4, Sangermano, Riccardo 5, Patankar, Sohil G. 5, Abdel-Hamid, Mohamed S. 6, AlAbdi, Lama 7, Safwat, Sylvia 8, 9, Flannery, Kyle P. 9, Dardas, Zain 3, Fatih, Jawid M. 3, Murali, Chaya 3, Kannan, Varun 1, Lotze, Timothy E. 1, Herman, Isabella 1, 2, 3, 10, Ammouri, Farah 10, 11, Rezich, Brianna 12, Efthymiou, Stephanie 13, Alavi, Shahryar 13, Murphy, David 14, Firoozfar, Zahra 15, Nasab, Mahya Ebrahimi 16, 17, Bahreini, Amir 18, 19, Ghasemi, Majid 20, Haridy, Nourelhoda A. 21, Goldouzi, Hamid Reza 22, Eghbal, Fatemeh 23, Karimiani, Ehsan Ghayoor 24, Begtrup, Amber 25, Elloumi, Houda 25, Srinivasan, Varunvenkat M. 26, Gowda, Vykuntaraju K. 26, Du, Haowei 3, Jhangiani, Shalini N. 27, Coban-Akdemir, Zeynep 3, 28, Marafi, Dana 3, 29, Rodan, Lance 30, 31, Isikay, Sedat 32, Rosenfeld, Jill A. 3, 33, Ramanathan, Subhadra 34, Staton, Michael 34, Oberg, Kerby C. 35, Clark, Robin D. 34, Wenman, Catharina 36, Loughlin, Sam 36, Saad, Ramy 37, Ashraf, Tazeen 37, Male, Alison 37, Tadros, Shereen 37, 38, Boostani, Reza 39, Abdel-Salam, Ghada M.H. 40, Zaki, Maha 40, Mardi, Ali 41, Hashemi-Gorji, Farzad 42, Abdalla, Ebtesam 8, Manzini, M. Chiara 9, Pehlivan, Davut 1, 2, 3, Posey, Jennifer E. 3, Gibbs, Richard A. 3, 27, Houlden, Henry 13, Alkuraya, Fowzan S. 43, 44, Bujakowska, Kinga 5, Maroofian, Reza 13, Lupski, James R. 2, 3, 27, 45, ∗∗, Nguyen, Long N. 4, 46, 47, 48, 49, ∗∗∗
Publikováno v:
In Genetics in Medicine January 2025 27(1)
Autor:
Maddirevula, Sateesh, Shagrani, Mohammad, Ji, Ae-Ri, Horne, Christopher R., Young, Samuel N., Mather, Lucy J., Alqahtani, Mashael, McKerlie, Colin, Wood, Geoffrey, Potter, Paul K., Abdulwahab, Firdous, AlSheddi, Tarfa, van der Woerd, Wendy L., van Gassen, Koen L.I., AlBogami, Dalal, Kumar, Kishwer, Muhammad Akhtar, Ali Syed, Binomar, Hiba, Almanea, Hadeel, Faqeih, Eissa, Fuchs, Sabine A., Scott, John W., Murphy, James M., Alkuraya, Fowzan S.
Publikováno v:
In Genetics in Medicine November 2024 26(11)
Autor:
Zhang, Yingzi, Bi, Chongwei, Nadeef, Seba, Maddirevula, Sateesh, Alqahtani, Mashael, Alkuraya, Fowzan S., Li, Mo
Publikováno v:
In Med 11 October 2024 5(10):1307-1325
Autor:
Roberts, Angharad M., DiStefano, Marina T., Riggs, Erin Rooney, Josephs, Katherine S., Alkuraya, Fowzan S., Amberger, Joanna, Amin, Mutaz, Berg, Jonathan S., Cunningham, Fiona, Eilbeck, Karen, Firth, Helen V., Foreman, Julia, Hamosh, Ada, Hay, Eleanor, Leigh, Sarah, Martin, Christa L., McDonagh, Ellen M., Perrett, Daniel, Ramos, Erin M., Robinson, Peter N., Rath, Ana, Sant, David W., Stark, Zornitza, Whiffin, Nicola, Rehm, Heidi L., Ware, James S.
Publikováno v:
In Genetics in Medicine February 2024 26(2)
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Akademický článek
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Autor:
AlAbdi, Lama 1, 20, Maddirevula, Sateesh 2, 20, Aljamal, Bayan 1, Hamid, Halima 3, Almulhim, Aisha 3, Hashem, Mais O. 1, Algoos, Yusra 1, Alqahtani, Mashael 1, Albaloshi, Shahad 1, Alghamdi, Mohammed 1, Alduaylij, Mohammed 1, Shamseldin, Hanan E. 1, Nadeef, Seba 1, Patel, Nisha 1, Abdulwahab, Firdous 1, Abouyousef, Omar 1, Alshidi, Tarfa 1, Jaafar, Amal 1, Abouelhoda, Mohamed 4, Alhazzani, Adel 6, Alfares, Ahmed 2, Qudair, Ahmad 7, Alsulaiman, Ahood 8, Alhashem, Amal 5, 9, 10, Khan, Arif O. 11, 12, Chedrawi, Aziza 8, Alebdi, Basel 1, AlAjlan, Fahad 6, Alotaibi, Fawaz 6, Alzaidan, Hamad 8, Banjar, Hanaa 13, Abdelraouf, Hanem 5, Alkuraya, Hisham 14, Abumansour, Iman 7, 15, Alfayez, Khowlah 5, Tulbah, Maha 16, Alowain, Mohammed 8, 9, Alqahtani, Mohammed 6, El-Kalioby, Mohammed 4, Shboul, Mohammad 17, Sulaiman, Raashda 8, Al Tala, Saed 18, Khan, Sameena 6, Coskun, Serdar 19, Mrouge, Sobaihi 7, Alenazi, Walaa 4, Rahbeeni, Zuhair 8, Alkuraya, Fowzan S. 1, 5, 21, ∗
Publikováno v:
In Med October 2024