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Browsing by Author Shieh, JT
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Showing results 3 to 5 of 5
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Title
Author(s)
Issue Date
Hnrnpa1 Mutations Cause Congenital Heart Defects
Proceeding/Conference:
Hong Kong Inter-University Postgraduate Symposium in Biochemical Sciences, 2017
Yu, Z
Tang, PLF
Wang, J
Bao, S
Shieh, JT
Leung, AWL
Zhang, Z
Gao, F
Wong, SYY
Hui, ALC
Gao, Y
Dung, NWF
Zhang, ZG
Fan, Y
Zhou, X
Zhang, Y
Wong, DSM
Sham, PC
Azhar, A
Kwok, PY
Tam, PPL
Lian, Q
Cheah, KSE
Wang, B
Song, Y
2017
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis
Journal:
Brain
Mak, CCY
Doherty, D
Lin, AE
Vegas, N
Cho, MT
Viot, G
Dimartino, C
Weisfeld-Adams, JD
Lessel, D
Joss, S
Li, C
Gonzaga-Jauregui, C
Zarate, YA
Ehmke, N
Horn, D
Troyer, C
Kant, SG
Lee, Y
Ishak, GE
Leung, G
Barone Pritchard, A
Yang, S
Bend, EG
Filippini, F
Roadhouse, C
Lebrun, N
Mehaffey, MG
Martin, P-M
Apple, B
Millan, F
Puk, O
Hoffer, MJV
Henderson, LB
McGowan, R
Wentzensen, IM
Pei, S
Zahir, FR
YU, M
Gibson, WT
Senab, A
Steeves, M
Murrell, JR
Luettgen, S
Francisco, E
Strom, TM
Amlie-Wolf, L
Kaindl, AM
Wilson, WG
Halbach, S
Basel-Salmon, L
Lev-El, N
Denecke, J
Vissers, LELM
Radtke, K
Chelly, J
Zackai, E
Friedman, JM
Bamshad, MJ
Nickerson, DA
Reid, RR
Devriendt, K
Chae, JH
Stolerman, E
McDougall, C
Powis, Z
Bienvenu, T
Tan, TY
Orenstein, N
Dobyns, WB
Shieh, JT
Choi, M
Waggoner, D
Gripp, KW
Parker, MJ
Stoler, J
Lyonnet, S
Cormier-Daire, V
Viskochil, D
Hoffman, TL
Amiel, J
Chung, BHY
Gordon, CT
University of Washington Center for Mendelian Genomics
2020
Mutations in Hnrnpa1 cause congenital heart defects
Journal:
JCI insight
Yu, Z
Tang, PL
Wang, J
Bao, S
Shieh, JT
Leung, AW
Zhang, Z
Gao, F
Wong, SY
Hui, AL
Gao, Y
Dung, N
Zhang, ZG
Fan, Y
Zhou, X
Zhang, Y
Wong, DS
Sham, PC
Azhar, A
Kwok, PY
Tam, PP
Lian, Q
Cheah, KSE
Wang, B
Song, Y
2018