Reflections on an academic career

por Hall, Judith G.
Publicado 2017

A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with marfan and loeys–dietz syndrome...

por Rienhoff, Hugh Young, Yeo, Chang-Yeol, Morissette, Rachel, Khrebtukova, Irina, Melnick, Jonathan, Luo, Shujun, Leng, Nan, Kim, Yeon-Jin, Schroth, Gary, Westwick, John, Vogel, Hannes, McDonnell, Nazli, Hall, Judith G, Whitman, Malcolm
Publicado 2013

International multidisciplinary collaboration toward an annotated definition of arthrogryposis multiplex congenita

por Dahan‐Oliel, Noémi, Cachecho, Sarah, Barnes, Douglas, Bedard, Tanya, Davison, Ann M., Dieterich, Klaus, Donohoe, Maureen, Fąfara, Alicja, Hamdy, Reggie, Hjartarson, Helgi T., S. Hoffman, Naimisha, Kimber, Eva, Komolkin, Igor, Lester, Ruth, Pontén, Eva, van Bosse, Harold J. P., Hall, Judith G.
Publicado 2019

Novel pathogenic variants and genes for myopathies identified by whole exome sequencing

por Hunter, Jesse M, Ahearn, Mary Ellen, Balak, Christopher D, Liang, Winnie S, Kurdoglu, Ahmet, Corneveaux, Jason J, Russell, Megan, Huentelman, Matthew J, Craig, David W, Carpten, John, Coons, Stephen W, DeMello, Daphne E, Hall, Judith G, Bernes, Saunder M, Baumbach-Reardon, Lisa
Publicado 2015