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Author/Creator Dalton, Joline

1. Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A). Issue 9 (22nd August 2020)

Authors:
Jayakody, Himali; Zarei, Sanam; Nguyen, Huy; Dalton, Joline; Chen, Kelly; Hudgins, Louanne; Day, John; Withrow, Kara; Pandya, Arti; Teasley, Jean; Dobyns, William B; Mathews, Katherine D; Moore, Steven A
Journal:
Journal of neuropathology and experimental neurology
Issue:
Volume 79:Issue 9(2020)
Page Start:
998
Record Type:
Journal Article
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2. De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects. (22nd September 2017)

Authors:
Slavotinek, Anne; Risolino, Maurizio; Losa, Marta; Cho, Megan T; Monaghan, Kristin G; Schneidman-Duhovny, Dina; Parisotto, Sarah; Herkert, Johanna C; Stegmann, Alexander P A; Miller, Kathryn; Shur, Natasha; Chui, Jacqueline; Muller, Eric; DeBrosse, Suzanne; Szot, Justin O; Chapman, Gavin; Pachter...
Journal:
Human molecular genetics
Issue:
Volume 26:Number 24(2017:Dec. 15)
Page Start:
4849
Record Type:
Journal Article
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3. The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME. (15th December 2020)

Authors:
Senderek, Jan; Lassuthova, Petra; Kabzińska, Dagmara; Abreu, Lisa; Baets, Jonathan; Beetz, Christian; Braathen, Geir J.; Brenner, David; Dalton, Joline; Dankwa, Lois; Deconinck, Tine; De Jonghe, Peter; Dräger, Bianca; Eggermann, Katja; Ellis, Melina; Fischer, Carina; Stojkovic, Tanya; Herrmann, D...
Journal:
Neurology
Issue:
Volume 95:Number 24(2020)
Page Start:
Record Type:
Journal Article
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