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European Journal of Human Genetics : EJHG|July 12, 2002
Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retinaKrisztina Wutz, Christian Sauer, Eberhart Zrenner, et al.
Journal of Applied Genetics|April 5, 2013
First insights into the metagenome of Egyptian mummies using next-generation sequencingRabab Khairat, Markus Ball, Chun-Chi Hsieh Chang, 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.
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