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Journal of Medical Genetics|December 19, 2001
Distinct phenotypes distinguish the molecular classes of Angelman syndromeA C Lossie, M M Whitney, D Amidon, et al.
Human Reproduction (Oxford, England)|September 18, 2004
Blood lymphocyte chimerism associated with IVF and monochorionic dizygous twinning: case reportC A Williams, M R Wallace, K C Drury, et al.
Human Mutation|April 17, 1999
Analysis of CpG C-to-T mutations in neurofibromatosis type 1. Mutations in brief no. 129. OnlineS Krkljus, C R Abernathy, J S Johnson, et al.
Equine Veterinary Journal. Supplement|October 31, 2002
Speed associated with plasma pH, oxygen content, total protein and urea in an 80 km raceR M Hoffman, T M Hess, C A Williams, et al.
American Journal of Medical Genetics|April 29, 1998
Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiencyR T Zori, F Z Boyar, W N Williams, et al.
Clinical Genetics|February 16, 2002
A family with a grand-maternally derived interstitial duplication of proximal 15qF Z Boyar, M M Whitney, A C Lossie, et al.
Paediatrics and International Child Health|September 28, 2013
International collaboration on prevention of shaken baby syndrome - an ongoing project/interventionSue Foley, Zsuzsanna Kovács, Jenny Rose, et al.
The Review of Scientific Instruments|October 1, 2022
A knock-on deuteron imager for measurements of fuel and hotspot asymmetry in direct-drive inertial confinement fusion implosions (invited)H G Rinderknecht, P V Heuer, J Kunimune, et al.
Anti-Cancer Agents in Medicinal Chemistry|February 22, 2008
Plant polyphenolics as anti-invasive cancer agentsM E Bracke, B W A Vanhoecke, L Derycke, et al.
American Journal of Medical Genetics|January 20, 1997
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutationS Saitoh, K Buiting, S B Cassidy, et al.
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