15 research outputs found

    The Greatest Little Mother In The World

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    https://digitalcommons.library.umaine.edu/mmb-vp/5730/thumbnail.jp

    Joan of Arc They Are Calling You

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    While you are sleeping, Your France is weeping,Wake from your dreams, Maid of France.Her heart is bleeding;Are you unheeding?Come with the flame in your glance;Through the Gates of Heaven, with your sword in hand,Come your legions to command. CHORUSJoan of Arc, Joan of Arc,Do your eyes, from the skies, see the foe?Don\u27t you see the drooping Fleurdelis?Can\u27t you hear the tears of Normandy?Joan of Arc, Joan of Arc,Let your spirit guide us through;Come lead your France to victory;Joan of Arc, they are calling you. Joan of you. Alsace is sighing,Lorraine is crying,Their mother, France, looks to you.Her sons at Verdun;Bearing the burden,Pray for your coming anew;At the Gates of Heaven, do they bar your way?Souls that passed through yesterday

    We\u27re going to take the sword away from William [first line of chorus]

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    Performers: Willie WestonPiano and Voice (with lyrics

    We\u27re Going To Take The Sword Away From William

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    Photograph of Willie Weston; Illustration of soldiers with weaponshttps://scholarsjunction.msstate.edu/cht-sheet-music/5637/thumbnail.jp

    My Bill from Louisville

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    Gift of Dr. Mary Jane Esplen.Piano vocal [instrumentation]You all know my old beau [first line]My Bill from Louisville [first line of chorus]F [key]Moderato [tempo]Popular song [form/genre]Man suitcase bridge ; Willie Weston (photograph) [illustration]EH Pfeiffer [graphic artist]Publisher's advertisement on back cover [note

    Genetic Heterogeneity of Usher Syndrome: Analysis of 151 Families with Usher Type I

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    Usher syndrome type I is an autosomal recessive disorder marked by hearing loss, vestibular areflexia, and retinitis pigmentosa. Six Usher I genetic subtypes at loci USH1A–USH1F have been reported. The MYO7A gene is responsible for USH1B, the most common subtype. In our analysis, 151 families with Usher I were screened by linkage and mutation analysis. MYO7A mutations were identified in 64 families with Usher I. Of the remaining 87 families, who were negative for MYO7A mutations, 54 were informative for linkage analysis and were screened with the remaining USH1 loci markers. Results of linkage and heterogeneity analyses showed no evidence of Usher types Ia or Ie. However, one maximum LOD score was observed lying within the USH1D region. Two lesser peak LOD scores were observed outside and between the putative regions for USH1D and USH1F, on chromosome 10. A HOMOG χ(2)((1)) plot shows evidence of heterogeneity across the USH1D, USH1F, and intervening regions. These results provide conclusive evidence that the second-most-common subtype of Usher I is due to genes on chromosome 10, and they confirm the existence of one Usher I gene in the previously defined USH1D region, as well as providing evidence for a second, and possibly a third, gene in the 10p/q region
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