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Nature Genetics|December 2, 1999
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.
Cerebellum (London, England)|August 15, 2020
Consensus on Virtual Management of Vestibular Disorders: Urgent Versus Expedited CareAasef G Shaikh, Adolfo Bronstein, Sergio Carmona, et al.
American Journal of Human Genetics|May 8, 2012
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndromeMark J Rieder, Glenn E Green, Sarah S Park, et al.
Science (New York, N.Y.)|August 27, 2011
The shaping of modern human immune systems by multiregional admixture with archaic humansLaurent Abi-Rached, Matthew J Jobin, Subhash Kulkarni, et al.
Bioorganic & Medicinal Chemistry Letters|March 21, 2012
Design and synthesis of dihydrobenzofuran amides as orally bioavailable, centrally active γ-secretase modulatorsMartin Pettersson, Douglas S Johnson, Chakrapani Subramanyam, et al.
Genome Research|February 1, 2017
Improved genome assembly of American alligator genome reveals conserved architecture of estrogen signalingEdward S Rice, Satomi Kohno, John St John, et al.
Epilepsia|February 13, 2023
WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality riskKaren L Oliver, Marina Trivisano, Simone A Mandelstam, et al.
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