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Science (New York, N.Y.)|October 19, 1990
Temperature and Thermal Emissivity of the Surface of Neptune's Satellite TritonR M Nelson, W D Smythe, B D Wallis, et al.Arthritis and Rheumatism|August 18, 2001
Abnormalities in fibrillin 1-containing microfibrils in dermal fibroblast cultures from patients with systemic sclerosis (scleroderma)D D Wallis, F K Tan, C M Kielty, et al.European Urology Focus|February 26, 2023
Urologic Oncology Survivorship Guidelines: An Overview of the Evidence and the Current Implementation GapDavid-Dan Nguyen, Christopher J D Wallis, Neil E Fleshner, et al.Journal of the American Chemical Society|October 24, 2013
Chirality driven metallic versus semiconducting behavior in a complete series of radical cation salts based on dimethyl-ethylenedithio-tetrathiafulvalene (DM-EDT-TTF)Flavia Pop, Pascale Auban-Senzier, Arkadiusz Frąckowiak, et al.Chemical Communications (Cambridge, England)|January 17, 2020
Silica bound co-pillar[4+1]arene as a novel supramolecular stationary phaseSubbareddy Mekapothula, Matthew A Addicoat, David J Boocock, et al.Proceedings of the National Academy of Sciences of the United States of America|August 16, 1994
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneityM Muenke, F Gurrieri, C Bay, et al.American Journal of Human Genetics|November 1, 1995
Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndromeM Muenke, L J Bone, H F Mitchell, et al.Journal of Medical Genetics|January 24, 2007
Abnormal sterol metabolism in holoprosencephaly: studies in cultured lymphoblastsD Haas, J Morgenthaler, F Lacbawan, et al.American Journal of Medical Genetics|December 15, 1991
On lumping and splitting: a fetus with clinical findings of the oral-facial-digital syndrome type VI, the hydrolethalus syndrome, and the Pallister-Hall syndromeM Muenke, E D Ruchelli, L B Rorke, et al.American Journal of Human Genetics|August 27, 1998
Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domainK Gaudenz, E Roessler, N Quaderi, et al.Pageof 49