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Human Mutation|February 1, 2011
MLL2 mutation spectrum in 45 patients with Kabuki syndromeAimée D C Paulussen, Alexander P A Stegmann, Marinus J Blok, et al.
Research Square|November 24, 2025
A meta-model of low back pain to examine collective expert knowledge of the effects of treatments and their mechanismsJacek Cholewicki, Paul W Hodges, John M Popovich, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|May 19, 2026
A meta-model of low back pain to examine collective expert knowledge of treatment effects and their mechanismsJacek Cholewicki, Paul W Hodges, John M Popovich, et al.
Journal of Medical Genetics|December 4, 2009
Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individualsBenjamin D Solomon, Felicitas Lacbawan, Sandra Mercier, et al.
European Journal of Human Genetics : EJHG|June 10, 2010
The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genesAimée D C Paulussen, Constance T Schrander-Stumpel, Demis C J Tserpelis, et al.
European Journal of Human Genetics : EJHG|January 26, 2019
De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphismsSandra Jansen, Ilse M van der Werf, A Micheil Innes, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|April 26, 2020
Editor's Choice - Nationwide Analysis of Patients Undergoing Iliac Artery Aneurysm Repair in the NetherlandsHamid Jalalzadeh, Reza Indrakusuma, Mark J W Koelemay, et al.
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