يعرض 1 - 20 نتائج من 224 نتيجة بحث عن '"T van den Akker"', وقت الاستعلام: 0.64s تنقيح النتائج
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    المساهمون: Dollfus, Hélène, R Lilien, Marc, Maffei, Pietro, Verloes, Alain, Muller, Jean, M Bacci, Giacomo, Cetiner, Metin, T van den Akker, Erica L, Grudzinska Pechhacker, Monika, Testa, Francesco, Lacombe, Didier, F Stokman, Marijn, Simonelli, Francesca, Gouronc, Aurélie, Gavard, Amélie, M van Haelst, Mieke, Koenig, Jen, Rossignol, Sylvie, Bergmann, Carsten, Zacchia, Miriam, P Leroy, Bart, Mosbah, Héléna, M Van Eerde, Albertien, Mekahli, Djalila, Servais, Aude, Poitou, Christine, Valverde, Diana

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:001281335300001; journal:EUROPEAN JOURNAL OF HUMAN GENETICS; https://hdl.handle.net/11591/533869

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    المساهمون: Pediatrics, Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D), Graduate School, General Paediatrics, ANS - Cellular & Molecular Mechanisms, ANS - Complex Trait Genetics, ARD - Amsterdam Reproduction and Development, Paediatric Endocrinology, Human Genetics, ACS - Pulmonary hypertension & thrombosis

    المصدر: American Journal of Medical Genetics, Part A, 191(5), 1476-1478. Wiley-Liss Inc.
    American journal of medical genetics. Part A, 191(5), 1476-1478. Wiley-Liss Inc.
    Vos, N, Menke, L A, Mooij, C F, van den Akker, E L T, Alders, M & van Haelst, M M 2023, ' Severe early-onset overgrowth in a case of pseudohypoparathyroidism type 1b, caused by STX16 deletion ', American Journal of Medical Genetics, Part A, vol. 191, no. 5, pp. 1476-1478 . https://doi.org/10.1002/ajmg.a.63154

    مصطلحات موضوعية: Genetics, Genetics (clinical)

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