يعرض 1 - 3 نتائج من 3 نتيجة بحث عن '"Bilge A. Ozel"', وقت الاستعلام: 0.94s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing

    المؤلفون: Fernanda A. Correa, Marcela M. França, Qing Fang, Qianyi Ma, Tania A. Bachega, Andresa Rodrigues, Bilge A. Ozel, Jun Z. Li, Berenice B. Mendonca, Alexander A. L. Jorge, Luciani R. Carvalho, Sally A. Camper, Ivo J. P Arnhold

    المصدر: Archives of Endocrinology and Metabolism, Vol 61, Iss 6, Pp 633-636

    مصطلحات موضوعية: Medicine, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

    وصف الملف: electronic resource

    Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972017000600633&lng=en&tlng=en; https://doaj.org/toc/2359-4292

    URL الوصول: https://doaj.org/article/48c3d10eaf4b490c97149dbadc8fb15a

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  2. 2
    SAT-LB58 Molecular Investigation of Recessive Inheritance by Exome Sequencing of Patients With Congenital Hypopituitarism

    المؤلفون: Berenice B. Mendonca, Jun Li, Alexander A. L. Jorge, Ivo J.P. Arnhold, Peter Gergics, Luciani R. Carvalho, Bilge A. Ozel, Renata Kertsz, Sally A. Camper, Anna Flavia Figueredo Benedetti, Qing Fang, Nathalia Garcia Bianchi Pereira Ferreira, Joao Luiz do Oliveira Madeira, Qianyi Ma, Isabela Peixoto Biscotto

    المصدر: Journal of the Endocrine Society

    مصطلحات موضوعية: Genetics, Neuroendocrinology and Pituitary, Recessive inheritance, business.industry, Endocrinology, Diabetes and Metabolism, Medicine, Congenital hypopituitarism, Hypothalamic-Pituitary Development and Function, business, medicine.disease, Exome sequencing, AcademicSubjects/MED00250

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb2263cc1dbff4cc42392742566cf2ee
    http://europepmc.org/articles/PMC7208499

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  3. 3
    Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing

    المؤلفون: Bilge A. Ozel, Tania A. S. S. Bachega, Luciani R. Carvalho, Qing Fang, Andresa Rodrigues, Sally A. Camper, Qianyi Ma, Fernanda A. Correa, Ivo J.P. Arnhold, Jun Li, Berenice B. Mendonca, Marcela M. França, Alexander A. L. Jorge

    المصدر: Archives of Endocrinology and Metabolism v.61 n.6 2017
    Arquivos de Endocrinologia e Metabolismo
    Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
    instacron:SBEM
    Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
    Universidade de São Paulo (USP)
    instacron:USP
    Archives of Endocrinology and Metabolism, Volume: 61, Issue: 6, Pages: 633-636, Published: DEC 2017
    Archives of Endocrinology and Metabolism, Vol 61, Iss 6, Pp 633-636

    مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, lcsh:Medicine, 030209 endocrinology & metabolism, lcsh:Diseases of the endocrine glands. Clinical endocrinology, Short stature, Article, Growth hormone deficiency, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Internal medicine, Medicine, Congenital adrenal hyperplasia, DOENÇAS DO DESENVOLVIMENTO ÓSSEO, Exome sequencing, Sanger sequencing, lcsh:RC648-665, medicine.diagnostic_test, business.industry, lcsh:R, ACTH stimulation test, Bone age, medicine.disease, 030104 developmental biology, Endocrinology, symbols, IGHD, medicine.symptom, business

    وصف الملف: text/html

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9cdab07d2724d8a242b43f59de4816e
    http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972017000600633

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