Adelaide Research & Scholarship: Browsing DSpace

Browsing "Medicine" by Author Ha, T.

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:

Showing results 7 to 11 of 11 < previous

Preview	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.

Showing results 7 to 11 of 11 < previous