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Human Molecular Genetics|August 24, 2005
Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsyHannes Lohi, Leonarda Ianzano, Xiao-Chu Zhao, et al.
Molecular Cytogenetics|March 22, 2014
Adult expression of a 3q13.31 microdeletionChelsea Lowther, Gregory Costain, Rebecca Melvin, et al.
Anesthesiology|January 1, 1995
Volumetric capnography in children. Influence of growth on the alveolar plateau slopeR S Ream, M S Schreiner, J D Neff, et al.
Respiration Physiology|June 1, 1992
Modelling steady state pulmonary elimination of He, SF6 and CO2: effect of morphometryG R Neufeld, J D Schwardt, S R Gobran, et al.
Blood|March 15, 1997
Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemiasK Fischer, S Fröhling, S W Scherer, et al.
Clinical Genetics|June 14, 2000
Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiencyM J Nowaczyk, M J Huggins, D J Tomkins, et al.
Nuclear Medicine Communications|May 11, 1999
Gated metabolic positron emission tomography (GAPET) of the myocardium: 18F-FDG-PET to optimize recognition of myocardial hibernationG Hör, W T Kranert, F D Maul, et al.
Human Molecular Genetics|April 23, 2004
Laforin preferentially binds the neurotoxic starch-like polyglucosans, which form in its absence in progressive myoclonus epilepsyElayne M Chan, Cameron A Ackerley, Hannes Lohi, et al.
Nature Genetics|August 3, 2004
Detection of large-scale variation in the human genomeA John Iafrate, Lars Feuk, Miguel N Rivera, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Variation in the AU(AT)-rich element within the 3'-untranslated region of PPP1R3 is associated with variation in plasma glucose in aboriginal CanadiansR A Hegele, S B Harris, B Zinman, et al.
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