يعرض 1 - 2 نتائج من 2 نتيجة بحث عن '"FOXC2 and FOXL1 genes"', وقت الاستعلام: 0.97s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotype

    المؤلفون: Xuezhen Wang, Lili Guo, Bei Zhang, Jiebin Wu, Yu Sun, Huimin Tao, Jing Sha, Jingfang Zhai, Min Liu

    المصدر: Molecular Cytogenetics, Vol 15, Iss 1, Pp 1-8 (2022)

    مصطلحات موضوعية: ACDMPV, LDS, Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes, Multiple-system structural malformations, Prenatal diagnosis, Genetics, QH426-470

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/1755-8166

    URL الوصول: https://doaj.org/article/da052e98810b4dc892e1a5f6c03fe7aa

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  2. 2
    دورية أكاديمية
    Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotype

    المؤلفون: Wang, XuezhenAff1, Aff2, Guo, LiliAff1, Aff2, Zhang, BeiAff1, Aff2, Aff3, Wu, JiebinAff1, Aff2, Aff3, Sun, YuAff3, Aff4, Tao, HuiminAff2, Aff3, Sha, Jing, Zhai, JingfangAff1, Aff2, Aff3, IDs13039022006279_cor8, Liu, MinAff2, Aff3, IDs13039022006279_cor9

    المصدر: Molecular Cytogenetics. 15(1)

    Find this article in full text from Springer Verlag. Find this article in full text from ProQuest Full Text Finder
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