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American Journal of Human Genetics|September 8, 2009
FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndromeAnas M Alazami, Ranad Shaheen, Fatema Alzahrani, et al.Archives of Microbiology|October 1, 2005
Cereulide-producing strains of Bacillus cereus show diversityCamelia Apetroaie, Maria A Andersson, Cathrin Spröer, et al.Genome Research|January 7, 2014
Genomic analysis of primordial dwarfism reveals novel disease genesRanad Shaheen, Eissa Faqeih, Shinu Ansari, et al.American Journal of Medical Genetics. Part A|March 14, 2009
Allelic heterogeneity in inbred populations: the Saudi experience with Alström syndrome as an illustrative exampleMohamed A Aldahmesh, Leen Abu-Safieh, Arif O Khan, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2016
Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burdenMohamed Abouelhoda, Turki Sobahy, Mohamed El-Kalioby, et al.Genome Biology|January 13, 2016
FBXO32, encoding a member of the SCF complex, is mutated in dilated cardiomyopathyNadya Al-Yacoub, Ranad Shaheen, Salma Mahmoud Awad, et al.Journal of Medical Genetics|October 12, 2012
Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutationRanad Shaheen, Anas M Alazami, Muneera J Alshammari, et al.Human Genetics|February 20, 2019
PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephalyRanad Shaheen, Monika Tasak, Sateesh Maddirevula, et al.Genome Biology|September 30, 2015
Mutation in WDR4 impairs tRNA m(7)G46 methylation and causes a distinct form of microcephalic primordial dwarfismRanad Shaheen, Ghada M H Abdel-Salam, Michael P Guy, et al.Journal of Medical Genetics|April 27, 2013
Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismusAnas M Alazami, Hadia Hijazi, Mohammed S Al-Dosari, et al.Pageof 9