受强制性开放获取政策约束的文章 - David John Amor了解详情
无法在其他位置公开访问的文章：23 篇
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Speech and language in children with Klinefelter syndrome
M St John, C Ponchard, O van Reyk, C Mei, L Pigdon, DJ Amor, ...
Journal of Communication Disorders 78, 84-96, 2019
强制性开放获取政策： National Health and Medical Research Council, Australia
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Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo‐obstruction
G Ravenscroft, S Pannell, G O'Grady, R Ong, HC Ee, F Faiz, L Marns, ...
Neurogastroenterology & Motility 30 (9), e13371, 2018
强制性开放获取政策： National Health and Medical Research Council, Australia
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Alcohol consumption in a general antenatal population and child neurodevelopment at 2 years
JL Halliday, E Muggli, S Lewis, EJ Elliott, DJ Amor, C O’Leary, S Donath, ...
J Epidemiol Community Health 71 (10), 990-998, 2017
强制性开放获取政策： National Health and Medical Research Council, Australia
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Expansion of phenotype of DDX3X syndrome: six new cases
B Beal, I Hayes, J McGaughran, DJ Amor, C Miteff, V Jackson, O van Reyk, ...
Clinical dysmorphology 28 (4), 169-174, 2019
强制性开放获取政策： National Health and Medical Research Council, Australia
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IREB2-associated neurodegeneration
MS Cooper, Z Stark, S Lunke, T Zhao, DJ Amor
Brain 142 (8), e40-e40, 2019
强制性开放获取政策： National Health and Medical Research Council, Australia
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Preferences for results from genomic microarrays: comparing parents and health care providers
E Turbitt, JL Halliday, DJ Amor, SA Metcalfe
Clinical Genetics 87 (1), 21-29, 2015
强制性开放获取政策： National Health and Medical Research Council, Australia
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Clinical comparison of overlapping deletions of 19p13. 3
H Risheg, R Pasion, S Sacharow, V Proud, LD Immken, S Schwartz, ...
American Journal of Medical Genetics Part A 161 (5), 1110-1116, 2013
强制性开放获取政策： Wellcome Trust
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The novel RAF1 mutation p.(Gly361Ala) located outside the kinase domain of the CR3 region in two patients with Noonan syndrome, including one with a rare …
FL Harms, M Alawi, DJ Amor, TY Tan, G Cuturilo, C Lissewski, ...
American Journal of Medical Genetics Part A 176 (2), 470-476, 2018
强制性开放获取政策： German Research Foundation, Federal Ministry of Education and Research, Germany
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Exome sequencing for isolated congenital hearing loss: a cost‐effectiveness analysis
L Downie, DJ Amor, J Halliday, S Lewis, M Martyn, I Goranitis
The Laryngoscope 131 (7), E2371-E2377, 2021
强制性开放获取政策： US National Institutes of Health
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DNA methylation analysis for screening and diagnostic testing in neurodevelopmental disorders
DE Godler, DJ Amor
Essays in Biochemistry 63 (6), 785-795, 2019
强制性开放获取政策： National Health and Medical Research Council, Australia, Medical Research …
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Feasibility of wearable technology for ‘real‐world’gait analysis in children with prader–willi and angelman syndromes
CM Kraan, P Date, A Rattray, M Sangeux, QM Bui, EK Baker, J Morison, ...
Journal of Intellectual Disability Research 66 (8-9), 717-725, 2022
强制性开放获取政策： National Health and Medical Research Council, Australia, Medical Research …
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Personal utility of genomic sequencing for infants with congenital deafness
E Tutty, DJ Amor, A Jarmolowicz, K Paton, L Downie
American Journal of Medical Genetics Part A 185 (12), 3634-3643, 2021
强制性开放获取政策： US National Institutes of Health
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Fragile females: case series of epilepsy in girls with FMR1 disruption
KA Myers, FNG van't Hof, LG Sadleir, G Legault, E Simard-Tremblay, ...
Pediatrics 144 (3), 2019
强制性开放获取政策： National Health and Medical Research Council, Australia, Citizen’s United …
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Anaplastic oligodendroglioma in an adolescent with Lynch syndrome
JA Heath, J Ng, V Beshay, L Coleman, P Lo, DJ Amor
Pediatric Blood & Cancer 60 (6), E13-E15, 2013
强制性开放获取政策： National Health and Medical Research Council, Australia
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The metabolic health of young men conceived using intracytoplasmic sperm injection
SR Catford, J Halliday, S Lewis, MK O’Bryan, DJ Handelsman, RJ Hart, ...
Human Reproduction 37 (12), 2908-2920, 2022
强制性开放获取政策： National Health and Medical Research Council, Australia
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An investigation of barriers and enablers for genetics in speech-language pathology explored through a case study of childhood apraxia of speech
ML Lauretta, A Jarmolowicz, DJ Amor, S Best, AT Morgan
Journal of Speech, Language, and Hearing Research 67 (9S), 3437-3451, 2024
强制性开放获取政策： National Health and Medical Research Council, Australia
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Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort
KR Dias, R Shrestha, D Schofield, CA Evans, E O’Heir, Y Zhu, F Zhang, ...
Genetics in Medicine 26 (5), 101076, 2024
强制性开放获取政策： National Health and Medical Research Council, Australia
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To speak may draw on epigenetic writing and reading: Unravelling the complexity of speech and language outcomes across chromatin-related neurodevelopmental disorders
M St John, T Tripathi, AT Morgan, DJ Amor
Neuroscience & Biobehavioral Reviews 152, 105293, 2023
强制性开放获取政策： National Health and Medical Research Council, Australia
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Dna Methylation Episignatures are Sensitive and Specific Biomarkers for Detection of Patients with Kat6A/Kat6B Variants
N Vos, J Reilly, MW Elting, PM Campeau, D Coman, Z Stark, TY Tan, ...
Epigenomics 15 (6), 351-367, 2023
强制性开放获取政策： Genome Canada
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Child health after preimplantation genetic testing
S Lewis, DJ Amor, A Glynn, L Wilton, J Halliday
Reproductive BioMedicine Online 42 (3), 609-619, 2021
强制性开放获取政策： National Health and Medical Research Council, Australia
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