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  1. Callen, Douglas Komponist; Cutolo, Cesare Komponist; Denning, Albert Komponist; Ellard, Fredrick Komponist; Ellard, William Komponist; Giorza, Paolo Komponist; Hatton, John Liptrot Komponist; Lavenu, Louis Komponist; Linger, Carl Komponist; Marsh, Henry Komponist; Marsh, Stephen Hale Alonzo Komponist; Miers, Charles J. Komponist; Robinson, William Cleaver Francis Komponist; Rochefort, Jean-Baptiste Komponist; Shield, William Komponist; Spagnoletti, Ernesto Komponist; Tate, James William Komponist; Wallace, William Vincent Komponist ; Victoria State Orchestra

    Vocal and Orchestral Music - ELLARD, F. / GIORZA, P. / LINGER, C. (Australia Unite!) (Quaife, W. Bolton, Victoria State Orchestra, Divall)

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    ABC Classics, 180102

    Published in: ABC Classics

  5. Garofalo, Silvio; Metsaranta, Marjo; Ellard, Jeffrey; Smith, Chad; Horton, William; Vuorio, Eero; de Crombrugghe, Benoit

    Assembly of Cartilage Collagen Fibrils is Disrupted by Overexpression of Normal Type II Collagen in Transgenic Mice

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    National Academy of Sciences of the United States of America, 1993

    Published in: Proceedings of the National Academy of Sciences of the United States of America

  8. Horton, William A.; Machado, Mirta A.; Ellard, Jeffrey; Campbell, Dianna; Bartley, James; Ramirez, Francesco; Vitale, Emilia; Lee, Brendan

    Characterization of a Type II Collagen Gene (COL2A1) Mutation Identified in Cultured Chondrocytes from Human Hypochondrogenesis

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    National Academy of Sciences of the United States of America, 1992

    Published in: Proceedings of the National Academy of Sciences of the United States of America

  15. Garofalo, Silvio; Vuorio, Eero; Metsaranta, Marjo; Rosati, Rita; Toman, David; Vaughan, Joe; Lozano, Guillermina; Mayne, Richard; Ellard, Jeff; Horton, William; de Crombrugghe, Benoit

    Reduced Amounts of Cartilage Collagen Fibrils and Growth Plate Anomalies in Transgenic Mice Harboring a Glycine-to-Cysteine Mutation in the Mouse Type II Procollagen α1-Chain Gene

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    National Academy of Sciences of the United States of America, 1991

    Published in: Proceedings of the National Academy of Sciences of the United States of America

  16. Wyatt, Rebecca C.; Hagopian, William A.; Roep, Bart O.; Patel, Kashyap A.; Resnick, Brittany; Dobbs, Rebecca; Hudson, Michelle; De Franco, Elisa; Ellard, Sian; Flanagan, Sarah E.; Hattersley, Andrew T.; Oram, Richard A.; Johnson, Matthew B.

    Congenital beta cell defects are not associated with markers of islet autoimmunity, even in the context of high genetic risk for type 1 diabetes

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    Springer Science and Business Media LLC, 2022

    Published in: Diabetologia

  17. Macken, William L.; Godwin, Annie; Wheway, Gabrielle; Stals, Karen; Nazlamova, Liliya; Ellard, Sian; Alfares, Ahmed; Aloraini, Taghrid; AlSubaie, Lamia; Alfadhel, Majid; Alajaji, Sulaiman; Wai, Htoo A.; Self, Jay; Douglas, Andrew G. L.; Kao, Alexander P.; Guille, Matthew; Baralle, Diana

    Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly

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    Springer Science and Business Media LLC, 2021

    Published in: Genome Medicine

  18. Harel, Shira; Cohen, Ana S.A.; Hussain, Khalid; Flanagan, Sarah E.; Schlade-Bartusiak, Kamilla; Patel, Millan; Courtade, Jaques; Li, Jenny B.W.; Van Karnebeek, Clara; Kurata, Harley; Ellard, Sian; Chanoine, Jean-Pierre; Gibson, William T.

    Alternating hypoglycemia and hyperglycemia in a toddler with a homozygous p.R1419H ABCC8 mutation: an unusual clinical picture

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    Walter de Gruyter GmbH, 2015

    Published in: Journal of Pediatric Endocrinology and Metabolism

  19. Rankin, Julia; Auer‐Grumbach, Michaela; Bagg, Warwick; Colclough, Kevin; Duong, Nguyen Thuy; Fenton‐May, Jane; Hattersley, Andrew; Hudson, Judith; Jardine, Philip; Josifova, Dragana; Longman, Cheryl; McWilliam, Robert; Owen, Katharine; Walker, Mark; Wehnert, Manfred; Ellard, Sian

    Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644C

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    Wiley, 2008

    Published in: American Journal of Medical Genetics Part A