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Nature Genetics|November 4, 2000
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat proteinC M Pusch, C Zeitz, O Brandau, et al.BMJ (Clinical Research Ed.)|December 19, 2012
Revisiting the harem conspiracy and death of Ramesses III: anthropological, forensic, radiological, and genetic studyZahi Hawass, Somaia Ismail, Ashraf Selim, et al.JAMA|February 18, 2010
Ancestry and pathology in King Tutankhamun's familyZahi Hawass, Yehia Z Gad, Somaia Ismail, et al.Nature Communications|October 3, 2020
A defect-resistant Co-Ni superalloy for 3D printingSean P Murray, Kira M Pusch, Andrew T Polonsky, et al.American Journal of Human Genetics|March 12, 2004
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4)Francesca Donaudy, Rik Snoeckx, Markus Pfister, et al.Neurology|December 7, 2007
Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraineB de Vries, T Freilinger, K R J Vanmolkot, et al.Nature Communications|March 20, 2012
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencingAndreas Keller, Angela Graefen, Markus Ball, et al.Pageof 12