يعرض 1 - 2 نتائج من 2 نتيجة بحث عن '"Khanh Thi Xuan Luong"', وقت الاستعلام: 0.61s تنقيح النتائج
  1. 1
    دورية أكاديمية
    CD40LG mutations in Vietnamese patients with X‐linked hyper‐IgM syndrome; catastrophic anti‐phospholipid syndrome as a new complication

    المؤلفون: Anh Nguyen Lien Phan, Thuy Thi Thanh Pham, Xinh Thi Phan, Nghia Huynh, Tuan Minh Nguyen, Cuc Tran Thu Cao, Duong Thuy Nguyen, Khanh Thi Xuan Luong, Tam Thi Minh Nguyen, Anh Ngoc Kim Tran, Linh Thi Truc Pham, Vy Vuong Thao Nguyen, Sigrid Swagemakers, Chi‐Bao Bui, Petrus Martinus Van Hagen

    المصدر: Molecular Genetics & Genomic Medicine, Vol 9, Iss 8, Pp n/a-n/a (2021)

    مصطلحات موضوعية: anti‐phospholipid syndrome, CD40 ligand, hyper‐IgM syndrome, primary immunodeficiency, whole‐exome sequencing, Genetics, QH426-470

    وصف الملف: electronic resource

    العلاقة: https://doaj.org/toc/2324-9269Test

    الوصول الحر: https://doaj.org/article/0ec76ae80e114e07ab80a8c6c31d35d3Test

    View record in DOAJ النص الكامل

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  2. 2
    CD40LG mutations in Vietnamese patients with X‐linked hyper‐IgM syndrome; catastrophic anti‐phospholipid syndrome as a new complication

    المؤلفون: Linh Thi Truc Pham, Xinh Thi Phan, Thuy Thi Thanh Pham, Vy Nguyen, Tuan Minh Nguyen, Anh Tran, Anh Nguyen Lien Phan, Sigrid M. A. Swagemakers, Petrus Martinus van Hagen, Khanh Thi Xuan Luong, Nghia Huynh, Tam Thi Minh Nguyen, Chi-Bao Bui, Cuc Tran Thu Cao, Duong Thuy Nguyen

    المساهمون: Pathology, Internal Medicine, Immunology

    المصدر: Molecular Genetics & Genomic Medicine
    Molecular Genetics and Genomic Medicine, 9(8):e1732. John Wiley & Sons Inc.
    Molecular Genetics & Genomic Medicine, Vol 9, Iss 8, Pp n/a-n/a (2021)

    مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Hyper IgM syndrome, anti‐phospholipid syndrome, Adolescent, CD40 Ligand, QH426-470, 030105 genetics & heredity, medicine.disease_cause, primary immunodeficiency, Clinical Reports, 03 medical and health sciences, Western blot, Genotype, Genetics, medicine, Humans, Child, Molecular Biology, CD40 ligand, Genetics (clinical), Exome sequencing, Mutation, Clinical Report, medicine.diagnostic_test, business.industry, Hyper-IgM Immunodeficiency Syndrome, Type 1, hyper‐IgM syndrome, medicine.disease, Antiphospholipid Syndrome, 030104 developmental biology, Otitis, Phenotype, Immunology, Primary immunodeficiency, whole‐exome sequencing, medicine.symptom, Complication, business

    وصف الملف: application/pdf

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db0f8bd5d9220d5f640107882e121896Test
    http://europepmc.org/articles/PMC8404229Test


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