HKU Scholars Hub: Browsing DSpace

Browsing "Department of Paediatrics & Adolescent Medicine" by Author innes, am

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 中

or enter first few letters:

Showing results 5 to 8 of 8 < previous

	Title	Author(s)	Issue Date	Views
	MSTO1 Mutations Cause Mtdna Depletion, Manifesting As Muscular Dystrophy With Cerebellar Involvement Journal:Acta Neuropathologica	Donkervoort, S Sabouny, R Yun, P Gauquelin, L Chao, KR Hu, Y AI Khatib, I Topf, A Mohassel, P Cummings, BB Kaur, R Saade, D Moore, SA Waddell, LB Farrar, MA Goodrich, JK Uapinyoying, P Chan, SHS Javed, A Leach, ME Karachunski, P Dalton, J Medne, L Harper, A Thompson, C Thiffault, I Specht, S Lamont, RE Saunders, C Racher, H Bernier, FP Mowat, D Witting, N Vissing, J Hanson, R Coffman, KA Hainlen, M Parboosingh, JS Carnevale, A Yoon, G Schnur, RE Care4Rare Canada Consortium Boycott, KM Mah, JK Straub, V Reghan Foley, A Innes, AM Bönnemann, CG Shutt, TE	2019	50
	Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia Journal:American Journal of Human Genetics	CamposXavier, AB Martinet, D Bateman, J Belluoccio, D Rowley, L Tan, TY Baxová, A Gustavson, KH Borochowitz, ZU Innes, AM Unger, S Beckmann, JS Mittaz, L Ballhausen, D SupertiFurga, A Savarirayan, R Bonafé, L	2009	70
	Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development Journal:Neuron	Lennox, AL Hoye, ML Jiang, R Johnson-Kerner, BL Suit, LA Venkataramanan, S Sheehan, CJ Alsina, FC Fregeau, B Aldinger, KA Moey, C Lobach, I Afenjar, A Babovic-Vuksanovic, D Bezieau, S Blackburn, PR Bunt, J Burglen, L Campeau, PM Charles, P Chung, BHY Cogne, B Curry, C D'Agostino, MD Di Donato, N Faivre, L Heron, D Innes, AM Isidor, B Keren, B Kimball, A Klee, EW Kuentz, P Kury, S Martin-Coignard, D Mirzaa, G Mignot, C Myake, N Matsumoto, N Fujita, A Nava, C Nizon, M Rodriguez, D Blok, LS Thauvin-Robinet, C Thevenon, J Vincent, M Ziegler, A Dobyns, W Richards, LJ Barkovich, AJ Floor, SN Silver, DL Sherr, EH	2020	43
	Williams-Beuren syndrome in diverse populations Journal:American Journal of Medical Genetics Part A	Kruszka, P Porras, AR de Souza, DH Moresco, A Huckstadt, V Gill, AD Goyle, AP Hu, T Addissie, YA Mok, TKG Tekendo-Ngongang, C Fieggen, K Prijoles, EJ Tanpaiboon, P Honey, E Luk, HM Lo, FMI Thong, MK Muthukumarasamy, P Jones, KL Belhassan, K Ouldim, K El Bouchikhi, I Bouguenouch, L Shukla, A Girisha, KM Sirisena, ND Dissanayake, VHW Paththinige, CS Mirshra, R Kislling, MS Ferreira, CR de Herreros, MB Lee, NC Jamuar, SS Lai, A Tan, ES Lim, JY Cham Breaba, WM Gupta, N Lotz-Esquivel, S Badilla-Porras, R Hussen, DF El Ruby, MO Ashaat, EA Patil, SJ Dowsett, L Eaton, A Innes, AM Shotelersuk, V Badoe, E Wonkam, A Obregon, MG Chung, BHY Trubnykova, M La Serna, J Gallardo Jugo, BE Chavez Pastor, M Abarca Barriga, HH Megarbane, A Kozel, BA van Haelst, MM Stevenson, RE Summar, M Adeyemo, AA Morris, CA Moretti-Ferreira, D Linguraru, MG Muenke, M	2018

Showing results 5 to 8 of 8 < previous