Zobrazeno 1 - 10
of 36
pro vyhledávání: '"TAIBAH, KHALID"'
Autor:
Greene, Daniel, Genomics England Research Consortium, Pirri, Daniela, Frudd, Karen, Sackey, Ege, Al-Owain, Mohammed, Giese, Arnaud PJ, Ramzan, Khushnooda, Riaz, Sehar, Yamanaka, Itaru, Boeckx, Nele, Thys, Chantal, Gelb, Bruce D, Brennan, Paul, Hartill, Verity, Harvengt, Julie, Kosho, Tomoki, Mansour, Sahar, Masuno, Mitsuo, Ohata, Takako, Stewart, Helen, Taibah, Khalid, Turner, Claire LS, Imtiaz, Faiqa, Riazuddin, Saima, Morisaki, Takayuki, Ostergaard, Pia, Loeys, Bart L, Morisaki, Hiroko, Ahmed, Zubair M, Birdsey, Graeme M, Freson, Kathleen, Mumford, Andrew, Turro, Ernest
Publikováno v:
Nature Medicine, 29, 3, pp. 679-688
Nature Medicine, 29, 679-688
Nature medicine
Nature Medicine, 29, 679-688
Nature medicine
Acknowledgements: This research was made possible through access to the data and findings generated by the 100,000 Genomes Project. The 100,000 Genomes Project is managed by Genomics England Limited (a wholly owned company of the Department of Health
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59a03cc9c8c028ea67cd79c4f4fd8438
Autor:
Ramzan, Khushnooda, Imtiaz, Faiqa, Taibah, Khalid, Alnufiee, Samir, Akhtar, Mohammed, Al-Hazzaa, Selwa A.F., Al-Owain, Mohammed
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology March 2014 78(3):427-432
Autor:
Al-Shaikh Abdulmoneem H, Sogaty Sameera, Al-Mostafa Abeer, Allam Rabab, Trabzuni Daniah, Al-Mubarak Bashayer, Kennedy Shelley, Bin-Khamis Ghada, Ramzan Khushnooda, Taibah Khalid, Imtiaz Faiqa, Bamukhayyar Saeed S, Meyer Brian F, Al-Owain Mohammed
Publikováno v:
BMC Medical Genetics, Vol 12, Iss 1, p 91 (2011)
Abstract Background Hearing loss is a clinically and genetically heterogeneous disorder. Mutations in the DFNB1 locus have been reported to be the most common cause of autosomal recessive non-syndromic hearing loss worldwide. Apart from DFNB1, many o
Externí odkaz:
https://doaj.org/article/7cc7b30f3f204eda8d3a587f734759c3
Autor:
Imtiaz, Faiqa1 fahmad@kfshrc.edu.sa, Taibah, Khalid2, Ramzan, Khushnooda1, Bin-Khamis, Ghada3, Kennedy, Shelley4, Al-Mubarak, Bashayer1, Trabzuni, Daniah1, Allam, Rabab1, Al-Mostafa, Abeer1, Sogaty, Sameera5, Al-Shaikh, Abdulmoneem H.6, Bamukhayyar, Saeed S.7, Meyer, Brian F.1, Al-Owain, Mohammed8,9
Publikováno v:
BMC Medical Genetics. 2011, Vol. 12 Issue 1, p91-96. 6p.
Autor:
TAIBAH, KHALID1 ktaibah@yahoo.com
Publikováno v:
Cochlear Implants International: An Interdisciplinary Journal. 2009, Vol. 10 Issue 4, p218-228. 11p. 7 Color Photographs.
Autor:
Imtiaz, Faiqa, Taibah, Khalid, Bin-Khamis, Ghada, Kennedy, Shelley, Hemidan, Amal, Al-Qahtani, Faisal, Tabbara, Khalid, Mubarak, Bashayer Al, Ramzan, Khushnooda, Meyer, Brian F., Al-Owain, Mohammed
Publikováno v:
Molecular Vision
Purpose Usher syndrome (USH) is an autosomal recessive disorder divided into three distinct clinical subtypes based on the severity of the hearing loss, manifestation of vestibular dysfunction, and the age of onset of retinitis pigmentosa and visual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::391fdbbc362244f79debcb4b5c8224d3
http://europepmc.org/articles/PMC3413430
http://europepmc.org/articles/PMC3413430
Autor:
Ramzan, Khushnooda, Taibah, Khalid, Tahir, Asma I., Al-Tassan, Nada, Berhan, Amal, Khater, Ahmed M., Al-Hazzaa, Selwa A.F., Al-Owain, Mohammed, Imtiaz, Faiqa
Publikováno v:
In European Journal of Medical Genetics May-June 2014 57(6):253-258
Akademický článek
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Publikováno v:
Journal of Otolaryngology; May/Jun2002, Vol. 31 Issue 3, p189, 4p, 4 Black and White Photographs
Autor:
Gangopadhyay, Kunal, Taibah, Khalid
Publikováno v:
ENT: Ear, Nose & Throat Journal; Oct1996, Vol. 75 Issue 10, p681, 4p, 3 Black and White Photographs