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Adelaide Research & Scholarship
Adelaide Research & Scholarship
Browsing "Medicine" by Author Ha, T.
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Showing results 7 to 11 of 11
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Issue Date
Title
Author(s)
2019
Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment
Quartier, A.
;
Courraud, J.
;
Ha, T.
;
McGillivray, G.
;
Isidor, B.
;
Rose, K.
;
Drouot, N.
;
Savidan, M.-A.
;
Feger, C.
;
Jagline, H.
;
Chelly, J.
;
Shaw, M.
;
Laumonnier, F.
;
Gecz, J.
;
Mandel, J.-L.
;
Piton, A.
2020
Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndrome
Arts, P.
;
Garland, J.
;
Byrne, A.B.
;
Hardy, T.S.E.
;
Babic, M.
;
Feng, J.
;
Wang, P.
;
Ha, T.
;
King-Smith, S.L.
;
Schreiber, A.W.
;
Crawford, A.
;
Manton, N.
;
Moore, L.
;
Barnett, C.P.
;
Scott, H.S.
2020
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Brown, A.L.
;
Arts, P.
;
Carmichael, C.L.
;
Babic, M.
;
Dobbins, J.
;
Chong, C.-E.
;
Schreiber, A.W.
;
Feng, J.
;
Phillips, K.
;
Wang, P.P.S.
;
Ha, T.
;
Homan, C.C.
;
King-Smith, S.L.
;
Rawlings, L.
;
Vakulin, C.
;
Dubowsky, A.
;
Burdett, J.
;
Moore, S.
;
McKavanagh, G.
;
Henry, D.
;
et al.
2014
The relationship between hypotension, cerebral flow, and the surgical field during endoscopic sinus surgery
Ha, T.
;
van Renen, R.
;
Ludbrook, G.
;
Valentine, R.
;
Ou, J.
;
Wormald, P.
2022
Variable expressivity in a four-generation ACDMPV family with a non-coding hypermorphic SNV in trans to the frameshifting FOXF1 variant
Yıldız Bölükbaşı, E.
;
Karolak, J.A.
;
Szafranski, P.
;
Gambin, T.
;
Matsika, A.
;
McManus, S.
;
Scott, H.S.
;
Arts, P.
;
Ha, T.
;
Barnett, C.P.
;
Rodgers, J.
;
Stankiewicz, P.