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Books
Development of two markers for hygienic behaviour of honeybees / by Peter Oxley, Ben Oldroyd and Gladys Ho.
Author / Creator:Oxley, Peter.
Publisher:Barton, A.C.T. : Rural Industries Research and Development Corporation, 2008.
Date:2008.
Call Numbers:TQ043630
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Books
The white-haired girl : an opera in five acts / by Ho Ching-chih and Ting Yi ; translated by Yang Hsien-yi and Gladys Yang.
Author / Creator:He, Jingzhi, 1924-
Publisher:Peking : Foreign Languages Press, 1954.
Edition:1st ed.
Date:1954.
Call Numbers:T0081409
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Books
Monochromes : from Malevich to the present / essays, Barbara Rose ... [et al.] ; artworks, Abakanowicz ... [et al.] ; edited by Valeria Varas, Raul Rispa.
Publisher:Berkeley, CA : University of California Press, 2007.
Date:2007.
Call Numbers:NQ709.04007/4
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Pictures | Drawings
Artwork for The School Magazine, 1996-1998 / by Peter Sheehan
Author / Creator:Sheehan, Peter, 1964-
Date:1996-1998
Call Numbers:PXE 1715
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Books
Between the lines : international short stories of war / Pauletta Otis and Steven Kaplan, editors.
Publisher:Ninot, CO : University Press of Colorado, 1994.
Date:1994.
Call Numbers:N808.839358/2
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Pictures | Prints
Part A: Bookplates filed alphabetically by the owner of the bookplate, "A to O", 1891-1935
Date:1891-1935
Call Numbers:DL PX 184/Box 4/Folders 1-14
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Manuscripts | Clippings
Sub-series 1: Angus & Robertson book reviews in bound volumes, 1894-1970
Date:1894-1970
Call Numbers:MLMSS 3269/Box 478-531
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ArticlesPeer ReviewedFull Text
The role of exome sequencing in childhood interstitial or diffuse lung disease
Author / Creator:Temple, Suzanna E. L. ; Ho, Gladys ; Bennetts, Bruce ; Boggs, Kirsten ; Vidic, Nada ; Mowat, David ; Christodoulou, John ; Schultz, André ; Gayagay, Thet ; Roscioli, Tony ; Zhu, Ying ; Lunke, Sebastian ; Armstrong, David ; Harrison, Joanne ; Kapur, Nitin ; McDonald, Tim ; Selvadurai, Hiran ; Tai, Andrew ; Stark, Zornitza ; Jaffe, Adam
Publisher:London: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2022-09, Vol.17 (1), p.1-350, Article 350
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ArticlesPeer ReviewedFull Text
Newborn Genomic Sequencing Needs Confirmation but Not Repeating
Author / Creator:Bennetts, Bruce ; Ho, Gladys ; Shin, Sarah ; Cheong, Pak Leng ; Wotton, Tiffany ; Ranieri, Enzo ; Pirreca, Shelley
Publisher:Switzerland: MDPI AG
Journal title:Children (Basel), 2024-11, Vol.11 (11), p.1287
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ArticlesPeer ReviewedFull Text
In vitro read-through of phenylalanine hydroxylase (PAH) nonsense mutations using aminoglycosides: a potential therapy for phenylketonuria
Author / Creator:Ho, Gladys ; Reichardt, Juergen ; Christodoulou, John
Publisher:Dordrecht: Springer Netherlands
Journal title:Journal of inherited metabolic disease, 2013-11, Vol.36 (6), p.955-959
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ArticlesPeer ReviewedFull Text
Perspectives of people with inherited retinal diseases on ocular gene therapy in Australia: protocol for a national survey
Author / Creator:Mack, Heather G ; Chen, Fred K ; Grigg, John ; Jamieson, Robyn ; De Roach, John ; O’Hare, Fleur ; Britten-Jones, Alexis Ceecee ; McGuinness, Myra ; Tindill, Nicole ; Ayton, Lauren ; Cordero, Anai Gonzalez ; Edwards, Thomas L ; Hewitt, Alex W ; Ho, Gladys ; Hogden, Michael ; Kwan, Anthony ; Lamey, Tina ; Ma, Alan ; Mackey, David ; Martin, Keith R ; McLaren, Terri ; Nash, Benjamin ; Ruddle, Jon ; Simunovic, Matthew ; Sinnerbrink, Ingrid ; Taranath, Deepa Ajay ; Thompson, Jen ; White, Jaclyn
Publisher:England: British Medical Journal Publishing Group
Journal title:BMJ open, 2021-06, Vol.11 (6), p.e048361-e048361
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ArticlesPeer ReviewedFull Text
Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families
Author / Creator:Tanudisastro, Hope A. ; Holman, Katherine ; Ho, Gladys ; Farnsworth, Elizabeth ; Fisk, Katrina ; Gayagay, Thet ; Hackett, Emma ; Jenkins, Gemma ; Krishnaraj, Rahul ; Lai, Tiffany ; Wong, Karen ; Patel, Chirag ; Mallawaarachchi, Amali ; Mallett, Andrew J. ; Bennetts, Bruce ; Alexander, Stephen I. ; McCarthy, Hugh J.
Publisher:London: Nature Publishing Group UK
Journal title:Npj genomic medicine, 2021-03, Vol.6 (1), p.20-20, Article 20
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ArticlesPeer ReviewedFull Text
Challenges in Diagnosing Intermediate Maple Syrup Urine Disease by Newborn Screening and Functional Validation of Genomic Results Imperative for Reproductive Family Planning
Author / Creator:Sajeev, Mona ; Chin, Sharon ; Ho, Gladys ; Bennetts, Bruce ; Sankaran, Bindu Parayil ; Gutierrez, Bea ; Devanapalli, Beena ; Tolun, Adviye Ayper ; Wiley, Veronica ; Fletcher, Janice ; Fuller, Maria ; Balasubramaniam, Shanti
Publisher:Basel: MDPI AG
Journal title:International journal of neonatal screening, 2021-06, Vol.7 (2), p.25
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ArticlesPeer ReviewedFull Text
Genomic testing for children with interstitial and diffuse lung disease (chILD): parent satisfaction, understanding and health-related quality of life
Author / Creator:Kelada, Lauren ; Wakefield, Claire ; Vidic, Nada ; Armstrong, David S ; Bennetts, Bruce ; Boggs, Kirsten ; Christodoulou, John ; Harrison, Joanne ; Ho, Gladys ; Kapur, Nitin ; Lindsey-Temple, Suzanna ; McDonald, Tim ; Mowat, David ; Schultz, André ; Selvadurai, Hiran ; Tai, Andrew ; Jaffe, Adam
Publisher:England: British Thoracic Society
Journal title:BMJ open respiratory research, 2022-02, Vol.9 (1), p.e001139
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ArticlesPeer ReviewedFull Text
Cyclin-Dependent Kinase-Like 5 (CDKL5) Mutation Screening in Rett Syndrome and Related Disorders
Author / Creator:White, Rose ; Ho, Gladys ; Schmidt, Swetlana ; Scheffer, Ingrid E. ; Fischer, Alexandra ; Yendle, Simone C. ; Bienvenu, Thierry ; Nectoux, Juliette ; Ellaway, Carolyn J. ; Darmanian, Artur ; Tong, XingZhang ; Cloosterman, Desiree ; Bennetts, Bruce ; Kalra, Veena ; Fullston, Tod ; Gecz, Jozef ; Cox, Timothy C. ; Christodoulou, John
Publisher:Cambridge, UK: Cambridge University Press
Journal title:Twin research and human genetics, 2010-04, Vol.13 (2), p.168-178
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ArticlesPeer ReviewedFull Text
Does it help to train attention in dyslexic children: pilot case studies with a ten-session neurofeedback program
Author / Creator:Au, Alma ; Ho, Gladys S.M. ; Choi, Elizabeth W.M. ; Leung, Patrick ; Waye, Mary M.Y. ; Kang, Kenneth ; Au, Kit-yee
Publisher:Berlin: De Gruyter
Journal title:International journal on disability and human development : IJDHD, 2014-02, Vol.13 (1), p.45-54
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ArticlesPeer ReviewedFull Text
The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy
Author / Creator:Fehr, Stephanie ; Wilson, Meredith ; Downs, Jenny ; Williams, Simon ; Murgia, Alessandra ; Sartori, Stefano ; Vecchi, Marilena ; Ho, Gladys ; Polli, Roberta ; Psoni, Stavroula ; Bao, Xinhua ; de Klerk, Nick ; Leonard, Helen ; Christodoulou, John
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2013-03, Vol.21 (3), p.266-273
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ArticlesPeer ReviewedFull Text
Catastrophic chemotherapy toxicity leading to diagnosis of Fanconi anaemia due to FANCD1/BRCA2 during adulthood: description of an emerging phenotype
Author / Creator:Ip, Emilia ; McNeil, Catriona ; Grimison, Peter ; Scheinberg, Tahlia ; Tudini, Emma ; Ho, Gladys ; Scott, Rodney J ; Brown, Christina ; Sandroussi, Charbel ; Guitera, Pascale ; Spurdle, Amanda B ; Goodwin, Annabel
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2022-09, Vol.59 (9), p.912-915
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ArticlesPeer ReviewedFull Text
There is variability in the attainment of developmental milestones in the CDKL5 disorder
Author / Creator:Fehr, Stephanie ; Leonard, Helen ; Ho, Gladys ; Williams, Simon ; de Klerk, Nick ; Forbes, David ; Christodoulou, John ; Downs, Jenny
Publisher:England: BioMed Central Ltd
Journal title:Journal of neurodevelopmental disorders, 2015-01, Vol.7 (1), p.2-2, Article 2
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ArticlesPeer ReviewedFull Text
Revealing hidden genetic diagnoses in the ocular anterior segment disorders
Author / Creator:Ma, Alan ; Yousoof, Saira ; Grigg, John R. ; Flaherty, Maree ; Minoche, Andre E. ; Cowley, Mark J. ; Nash, Benjamin M. ; Ho, Gladys ; Gayagay, Thet ; Lai, Tiffany ; Farnsworth, Elizabeth ; Hackett, Emma L. ; Fisk, Katrina ; Wong, Karen ; Holman, Katherine J. ; Jenkins, Gemma ; Cheng, Anson ; Martin, Frank ; Karaconji, Tanya ; Elder, James E. ; Enriquez, Annabelle ; Wilson, Meredith ; Amor, David J. ; Stutterd, Chloe A. ; Kamien, Benjamin ; Nelson, John ; Dinger, Marcel E. ; Bennetts, Bruce ; Jamieson, Robyn V.
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2020-10, Vol.22 (10), p.1623-1632
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Showing 1 to 20 of 25 results

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Development of two markers for hygienic behaviour of honeybees / by Peter Oxley, Ben Oldroyd and Gladys Ho.

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The white-haired girl : an opera in five acts / by Ho Ching-chih and Ting Yi ; translated by Yang Hsien-yi and Gladys Yang.

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Monochromes : from Malevich to the present / essays, Barbara Rose ... [et al.] ; artworks, Abakanowicz ... [et al.] ; edited by Valeria Varas, Raul Rispa.

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Artwork for The School Magazine, 1996-1998 / by Peter Sheehan

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Between the lines : international short stories of war / Pauletta Otis and Steven Kaplan, editors.

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Part A: Bookplates filed alphabetically by the owner of the bookplate, "A to O", 1891-1935

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Sub-series 1: Angus & Robertson book reviews in bound volumes, 1894-1970

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The role of exome sequencing in childhood interstitial or diffuse lung disease

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Newborn Genomic Sequencing Needs Confirmation but Not Repeating

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In vitro read-through of phenylalanine hydroxylase (PAH) nonsense mutations using aminoglycosides: a potential therapy for phenylketonuria

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Perspectives of people with inherited retinal diseases on ocular gene therapy in Australia: protocol for a national survey

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Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families

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Challenges in Diagnosing Intermediate Maple Syrup Urine Disease by Newborn Screening and Functional Validation of Genomic Results Imperative for Reproductive Family Planning

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Genomic testing for children with interstitial and diffuse lung disease (chILD): parent satisfaction, understanding and health-related quality of life

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Cyclin-Dependent Kinase-Like 5 (CDKL5) Mutation Screening in Rett Syndrome and Related Disorders

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Does it help to train attention in dyslexic children: pilot case studies with a ten-session neurofeedback program

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The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy

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Catastrophic chemotherapy toxicity leading to diagnosis of Fanconi anaemia due to FANCD1/BRCA2 during adulthood: description of an emerging phenotype

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There is variability in the attainment of developmental milestones in the CDKL5 disorder

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Revealing hidden genetic diagnoses in the ocular anterior segment disorders

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