يعرض 1 - 19 نتائج من 19 نتيجة بحث عن '"Ozair Abawi"', وقت الاستعلام: 0.56s تنقيح النتائج
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    المصدر: van der Valk, E, Abawi, O, Mohseni, M, Abdelmoumen, A, Wester, V, van der Voorn, B, Iyer, A, van den Akker, E, Hoeks, S, van den Berg, S, de Rijke, Y, Stalder, T & van Rossum, E 2022, ' Cross-sectional relation of long-term glucocorticoids in hair with anthropometric measurements and their possible determinants : A systematic review and meta-analysis ', Obesity reviews, vol. 23, no. 3, e13376, pp. 1-21 . https://doi.org/10.1111/obr.13376

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    المساهمون: Pediatrics, Internal Medicine, Human genetics, Amsterdam Reproduction & Development (AR&D), Amsterdam Neuroscience - Complex Trait Genetics, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, ARD - Amsterdam Reproduction and Development, Graduate School, AII - Inflammatory diseases, Human Genetics, ACS - Pulmonary hypertension & thrombosis

    المصدر: European Journal of Endocrinology, 182(1), 47-56. Bioscientifica Ltd
    Kleinendorst, L, Abawi, O, van der Kamp, H J, Alders, M, Meijers-Heijboer, H E J, van Rossum, E F C, van den Akker, E L T & van Haelst, M M 2019, ' Leptin receptor deficiency : A systematic literature review and prevalence estimation based on population genetics ', European Journal of Endocrinology, vol. 182, no. 1, pp. 47-56 . https://doi.org/10.1530/EJE-19-0678
    European Journal of Endocrinology, 182(1), 47-56. BioScientifica Ltd.
    European journal of endocrinology / European Federation of Endocrine Societies, 182(1), 47-56. BioScientifica Ltd.

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    المساهمون: Human Genetics, Graduate School, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam Reproduction & Development (AR&D), Pediatrics, Human genetics, Amsterdam Neuroscience - Complex Trait Genetics

    المصدر: Eur J Hum Genet
    European journal of human genetics, 28(7), 943-946. Nature Publishing Group
    Kleinendorst, L, Alsters, S I M, Abawi, O, Waisfisz, Q, Boon, E M J, van den Akker, E L T & van Haelst, M M 2020, ' Second case of Bardet–Biedl syndrome caused by biallelic variants in IFT74 ', European Journal of Human Genetics, vol. 28, no. 7, pp. 943-946 . https://doi.org/10.1038/s41431-020-0594-z
    European Journal of Human Genetics, 28(7), 943-946. Nature Publishing Group

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