Sökresultat - Martin, Megan M

Selective hippocampal cholinergic deafferentation impairs self-movement cue use during a food hoarding task av Martin, Megan M., Wallace, Douglas G.

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Fractionating dead reckoning: role of the compass, odometer, logbook, and home base establishment in spatial orientation av Wallace, Douglas G., Martin, Megan M., Winter, Shawn S.

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Organization of food protection behavior is differentially influenced by 192 IgG-saporin lesions of either the medial septum or the nucleus basalis magnocellularis av Martin, Megan M., Winter, Shawn S., Cheatwood, Joseph L., Carter, Lynniece A., Jones, Jeana L., Weathered, Scott L., Wagner, Steven J., Wallace, Douglas G.

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Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Dis... av Ho, Karen S., Wassman, E. Robert, Baxter, Adrianne L., Hensel, Charles H., Martin, Megan M., Prasad, Aparna, Twede, Hope, Vanzo, Rena J., Butler, Merlin G.

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Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders av Ho, Karen S., Twede, Hope, Vanzo, Rena, Harward, Erin, Hensel, Charles H., Martin, Megan M., Page, Stephanie, Peiffer, Andreas, Mowery-Rushton, Patricia, Serrano, Moises, Wassman, E. Robert

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Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf–Hirschhorn syndrome av Ho, Karen S, South, Sarah T, Lortz, Amanda, Hensel, Charles H, Sdano, Mallory R, Vanzo, Rena J, Martin, Megan M, Peiffer, Andreas, Lambert, Christophe G, Calhoun, Amy, Carey, John C, Battaglia, Agatino

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Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing av Hensel, Charles H., Vanzo, Rena J., Martin, Megan M., Ling, Ling, Aliaga, Solange M., Bui, Minh, Francis, David I., Twede, Hope, Field, Michael H., Morison, Jonathon W., Amor, David J., Godler, David E.

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Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders av Wassman, E. Robert, Ho, Karen S., Bertrand, Diana, Davis, Kyle W., Martin, Megan M., Page, Stephanie, Peiffer, Andreas, Prasad, Aparna, Serrano, Moises A., Twede, Hope, Vanzo, Rena, Scherer, Stephen W., Uddin, Mohammed, Hensel, Charles H.

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