Found: 2

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  • Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.

    Published in:
    Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-020-00407-5
    By:
    • Yap, Chloe X.;
    • Alvares, Gail A.;
    • Henders, Anjali K.;
    • Lin, Tian;
    • Wallace, Leanne;
    • Farrelly, Alaina;
    • McLaren, Tiana;
    • Berry, Jolene;
    • Vinkhuyzen, Anna A. E.;
    • Trzaskowski, Maciej;
    • Zeng, Jian;
    • Yang, Yuanhao;
    • Cleary, Dominique;
    • Grove, Rachel;
    • Hafekost, Claire;
    • Harun, Alexis;
    • Holdsworth, Helen;
    • Jellett, Rachel;
    • Khan, Feroza;
    • Lawson, Lauren
    Publication type:
    Article

  • Sleep‐disordered breathing in Australian children with Prader‐Willi syndrome following initiation of growth hormone therapy.

    Published in:
    Journal of Paediatrics & Child Health, 2022, v. 58, n. 2, p. 248, doi. 10.1111/jpc.15691
    By:
    • Caudri, Daan;
    • Nixon, Gillian M;
    • Nielsen, Aleisha;
    • Mai, Linda;
    • Hafekost, Claire R;
    • Kapur, Nitin;
    • Seton, Chris;
    • Tai, Andrew;
    • Blecher, Greg;
    • Ambler, Geoff;
    • Bergman, Philip B;
    • Vora, Komal A;
    • Crock, Patricia;
    • Verge, Charles F;
    • Tham, Elaine;
    • Musthaffa, Yassmin;
    • Lafferty, Antony R;
    • Jacoby, Peter;
    • Wilson, Andrew C;
    • Downs, Jenny
    Publication type:
    Article