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Works (3)

“We are not a typical family anymore”: Exploring the experiences and support needs of fathers of children with Fragile X syndrome in Australia

American Journal of Medical Genetics Part A
2024-04 | Journal article
DOI: 10.1002/ajmg.a.63470
Contributors: Jacintha Luermans; Jane Fleming; Rosie O'Shea; Kristine Barlow‐Stewart; Elizabeth Emma Palmer; Melanie Leffler
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Further delineation of dosage‐sensitive K/L mediated Xq28 duplication syndrome includes incomplete penetrance

Clinical Genetics
2023-06 | Journal article
DOI: 10.1111/cge.14303
Contributors: Melanie Leffler; Louise Christie; Anna Hackett; Bruce Bennetts; Himanshu Goel; David J. Amor; Greg B. Peters; Michael Field; Tracy Dudding‐Byth
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IDMOD: An Australian microsimulation model of lifetime economic and social factors in familial intellectual disability

International Journal of Microsimulation
2020 | Journal article
DOI: 10.34196/ijm.00212
Contributors: Deborah J Schofield; Owen Tan; Rupendra N Shrestha; Radhika Rajkumar; Sarah West; Morgan Rice; Nadine Kasparian; Jackie Boyle; Louise Christie; Melanie Leffler et al.
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