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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2008
Increased genetic counseling support improves communication of genetic information in familiesLaura E Forrest, Jo Burke, Sonya Bacic, et al.
Genes|April 10, 2019
Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation AllelesAlison Pandelache, Emma K Baker, Solange M Aliaga, et al.
American Journal of Medical Genetics. Part A|February 5, 2021
Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening programAnna I Jarmolowicz, Emma K Baker, Essra Bartlett, et al.
The Journal of Pain|April 8, 2025
Methods to discriminate between nociceptive, neuropathic and nociplastic in children & adolescents: A systematic review of psychometric properties and feasibilityAayushi Khillan, Liam Carter, David J Amor, et al.
Reproductive Biomedicine Online|February 2, 2021
Child health after preimplantation genetic testingSharon Lewis, David J Amor, Anne Glynn, et al.
American Journal of Medical Genetics. Part A|July 27, 2025
Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2Lottie D Morison, Ruth Braden, David J Amor, et al.
Neuroscience and Biobehavioral Reviews|June 23, 2023
To speak may draw on epigenetic writing and reading: Unravelling the complexity of speech and language outcomes across chromatin-related neurodevelopmental disordersMiya St John, Tanya Tripathi, Angela T Morgan, et al.
Disability and Health Journal|October 15, 2024
Parents' perspectives on conversations about prognosis and an assessment of prognostic information available online: A mixed-methods studyAkira Gokoolparsadh, Meg Bourne, Alison McEwen, et al.
American Journal of Medical Genetics. Part A|June 29, 2021
Personal utility of genomic sequencing for infants with congenital deafnessErin Tutty, David J Amor, Anna Jarmolowicz, et al.
American Journal of Medical Genetics. Part A|August 30, 2007
Keipert syndrome (Nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2-Xq28David J Amor, Hans-Henrik M Dahl, Melanie Bahlo, et al.
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