Items where Author is "Newman, William G."

Article

Beaman, Glenda M. and Lopes, Filipa M. and Hofmann, Aybike and Roesch, Wolfgang and Promm, Martin and Bijlsma, Emilia K. and Patel, Chirag and Akinci, Aykut and Burgu, Berk and Knijnenburg, Jeroen and Ho, Gladys and Aufschlaeger, Christina and Dathe, Sylvia and Voelckel, Marie Antoinette and Cohen, Monika and Yue, Wyatt W. and Stuart, Helen M. and Mckenzie, Edward A. and Elvin, Mark and Roberts, Neil A. and Woolf, Adrian S. and Newman, William G. (2022) Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder. FRONTIERS IN GENETICS, 13: 896125. ISSN , 1664-8021

Rieke, Johanna Magdalena and Zhang, Rong and Braun, Doreen and Yilmaz, Oeznur and Japp, Anna S. and Lopes, Filipa M. and Pleschka, Michael and Hilger, Alina C. and Schneider, Sophia and Newman, William G. and Beaman, Glenda M. and Nordenskjoeld, Agneta and Ebert, Anne-Karoline and Promm, Martin and Roesch, Wolfgang H. and Stein, Raimund and Hirsch, Karin and Schaefer, Frank-Mattias and Schmiedeke, Eberhard and Boemers, Thomas M. and Lacher, Martin and Kluth, Dietrich and Gosemann, Jan-Hendrik and Anderberg, Magnus and Barker, Gillian and Holmdahl, Gundela and Laeckgren, Goran and Keene, David and Cervellione, Raimondo M. and Giorgio, Elisa and Di Grazia, Massimo and Feitz, Wouter F. J. and Marcelis, Carlo L. M. and Van Rooij, Iris A. L. M. and Boekenkamp, Arend and Beckers, Goedele M. A. and Keegan, Catherine E. and Sharma, Amit and Dakal, Tikam Chand and Wittler, Lars and Grote, Phillip and Zwink, Nadine and Jenetzky, Ekkehart and Brusco, Alfredo and Thiele, Holger and Ludwig, Michael and Schweizer, Ulrich and Woolf, Adrian S. and Odermatt, Benjamin and Reutter, Heiko (2020) SLC20A1Is Involved in Urinary Tract and Urorectal Development. FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 8: 567. ISSN 2296-634X

Wieczorek, Dagmar and Newman, William G. and Wieland, Thomas and Berulava, Tea and Kaffe, Maria and Falkenstein, Daniela and Beetz, Christian and Graf, Elisabeth and Schwarzmayr, Thomas and Douzgou, Sofia and Clayton-Smith, Jill and Daly, Sarah B. and Williams, Simon G. and Bhaskar, Sanjeev S. and Urquhart, Jill E. and Anderson, Beverley and O'Sullivan, James and Boute, Odile and Gundlach, Jasmin and Czeschik, Johanna Christina and van Essen, Anthonie J. and Hazan, Filiz and Park, Sarah and Hing, Anne and Kuechler, Alma and Lohmann, Dietmar R. and Ludwig, Kerstin U. and Mangold, Elisabeth and Steenpass, Laura and Zeschnigk, Michael and Lemke, Johannes R. and Lourenco, Charles Marques and Hehr, Ute and Prott, Eva-Christina and Waldenberger, Melanie and Boehmer, Anne C. and Horsthemke, Bernhard and O'Keefe, Raymond T. and Meitinger, Thomas and Bum, John and Luedecke, Hermann-Josef and Strom, Tim M. (2014) Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome. AMERICAN JOURNAL OF HUMAN GENETICS, 95 (6). pp. 698-707. ISSN 0002-9297, 1537-6605